Variant report

Variant	nsv947198
Chromosome Location	chr1:155206997-155226440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2296)
CpG islands
(count:2260)
Chromatin interactive
region (count:128)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2296 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155220551-155220817	K562	blood:	n/a	n/a
2	ARID3A	chr1:155225460-155225617	K562	blood:	n/a	n/a
3	ARID3A	chr1:155210932-155211354	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:155214261-155214791	K562	blood:	n/a	n/a
5	ARID3A	chr1:155220524-155221272	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:155211743-155211909	K562	blood:	n/a	n/a
7	ATF1	chr1:155214362-155214888	K562	blood:	n/a	n/a
8	ATF1	chr1:155210928-155211236	K562	blood:	n/a	n/a
9	ATF2	chr1:155210932-155211284	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:155220463-155220771	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:155214167-155214963	GM12878	blood:	n/a	n/a
12	ATF2	chr1:155214348-155214853	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:155220393-155220839	GM12878	blood:	n/a	n/a
14	ATF2	chr1:155220343-155220830	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:155210887-155211301	GM12878	blood:	n/a	n/a
16	ATF2	chr1:155225087-155225506	GM12878	blood:	n/a	n/a
17	ATF2	chr1:155210881-155211282	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr1:155214167-155215115	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr1:155214122-155214921	GM12878	blood:	n/a	n/a
20	ATF3	chr1:155214302-155215021	A549	lung:	n/a	chr1:155214946-155214957
21	ATF3	chr1:155210875-155211296	GM12878	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
22	ATF3	chr1:155214300-155214921	A549	lung:	n/a	n/a
23	ATF3	chr1:155210875-155211383	A549	lung:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
24	ATF3	chr1:155210897-155211162	GM12878	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
25	ATF3	chr1:155210871-155211264	H1-hESC	embryonic stem cell:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
26	ATF3	chr1:155210904-155211278	K562	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
27	ATF3	chr1:155210893-155211233	HepG2	liver:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
28	ATF3	chr1:155211444-155211871	K562	blood:	n/a	n/a
29	ATF3	chr1:155210895-155211289	H1-hESC	embryonic stem cell:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
30	ATF3	chr1:155210797-155211327	HepG2	liver:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
31	ATF3	chr1:155214207-155214816	K562	blood:	n/a	n/a
32	ATF3	chr1:155210878-155211279	A549	lung:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
33	ATF3	chr1:155210888-155211238	K562	blood:	n/a	chr1:155211080-155211089 chr1:155211060-155211069
34	BACH1	chr1:155225130-155225581	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr1:155214529-155214809	K562	blood:	n/a	n/a
36	BACH1	chr1:155220356-155220796	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr1:155214493-155214979	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr1:155214349-155214807	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:155214416-155214822	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:155214431-155214747	GM12878	blood:	n/a	n/a
41	BCL3	chr1:155210785-155211265	A549	lung:	n/a	chr1:155211090-155211099
42	BCL3	chr1:155214043-155215196	A549	lung:	n/a	n/a
43	BCL3	chr1:155225274-155225748	A549	lung:	n/a	n/a
44	BCL3	chr1:155225024-155225441	GM12878	blood:	n/a	n/a
45	BCL3	chr1:155214182-155214907	A549	lung:	n/a	n/a
46	BCL3	chr1:155214215-155214798	GM12878	blood:	n/a	n/a
47	BCL3	chr1:155210894-155211423	A549	lung:	n/a	chr1:155211090-155211099
48	BCLAF1	chr1:155225080-155225546	GM12878	blood:	n/a	n/a
49	BCLAF1	chr1:155214135-155214932	K562	blood:	n/a	n/a
50	BCLAF1	chr1:155220385-155220845	GM12878	blood:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155214492-155214542	AG09309	skin:	n/a
2	chr1:155225808-155225858	HepG2	liver:	n/a
3	chr1:155214838-155214888	HCT-116	colon:	n/a
4	chr1:155214492-155214542	AG09309	skin:	n/a
5	chr1:155225808-155225858	HepG2	liver:	n/a
6	chr1:155214838-155214888	HCT-116	colon:	n/a
7	chr1:155225142-155225192	GM12878	blood:	n/a
8	chr1:155208775-155208825	HUVEC	blood vessel:	n/a
9	chr1:155217830-155217880	HL-60	blood:	n/a
10	chr1:155220536-155220586	HCF	heart:	n/a
11	chr1:155213714-155213764	HL-60	blood:	n/a
12	chr1:155214564-155214614	GM12878	blood:	n/a
13	chr1:155214303-155214353	PrEC	prostate:	n/a
14	chr1:155226099-155226149	H1-hESC	embryonic stem cell:	embryo
15	chr1:155211079-155211129	SAEC	small airway:	n/a
16	chr1:155214859-155214909	HNPCEpiC	eye:	n/a
17	chr1:155214859-155214909	SK-N-SH	brain:	n/a
18	chr1:155225402-155225452	GM12892	blood:	n/a
19	chr1:155215158-155215208	HEEpiC	esophagus:	n/a
20	chr1:155225375-155225425	CMK	blood:	n/a
21	chr1:155214815-155214865	AG09309	skin:	n/a
22	chr1:155226127-155226177	H1-hESC	embryonic stem cell:	embryo
23	chr1:155214575-155214625	HCF	heart:	n/a
24	chr1:155226127-155226177	IMR90	lung:	fetal
25	chr1:155226099-155226149	HNPCEpiC	eye:	n/a
26	chr1:155214564-155214614	AG10803	skin:	n/a
27	chr1:155220231-155220281	A549	lung:	n/a
28	chr1:155214303-155214353	ovcar-3	ovarian:	n/a
29	chr1:155224863-155224913	ECC-1	luminal epithelium:	n/a
30	chr1:155214838-155214888	RPTEC	kidney:	n/a
31	chr1:155211079-155211129	HepG2	liver:	n/a
32	chr1:155220536-155220586	ovcar-3	ovarian:	n/a
33	chr1:155225385-155225435	MCF-7	breast:	n/a
34	chr1:155211736-155211786	AG10803	skin:	n/a
35	chr1:155225764-155225814	AG09319	gingival:	n/a
36	chr1:155226099-155226149	Caco-2	colon:	n/a
37	chr1:155218830-155218880	NH-A	brain:	n/a
38	chr1:155224769-155224819	HL-60	blood:	n/a
39	chr1:155208775-155208825	HRE	kidney:	n/a
40	chr1:155221277-155221327	ProgFib	skin:	n/a
41	chr1:155221277-155221327	LNCaP	prostate:	n/a
42	chr1:155223726-155223776	HUVEC	blood vessel:	n/a
43	chr1:155224863-155224913	HAEpiC	amniotic membrane:	n/a
44	chr1:155224842-155224892	AG09309	skin:	n/a
45	chr1:155220536-155220586	NHDF-neo	bronchial:	n/a
46	chr1:155224863-155224913	H1-hESC	embryonic stem cell:	embryo
47	chr1:155226099-155226149	GM19239	blood:	n/a
48	chr1:155215158-155215208	K562	blood:	n/a
49	chr1:155213747-155213797	HEK293	kidney:	embryo
50	chr1:155223726-155223776	NB4	blood:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:155220572..155221167-chr1:155276946..155277691,3	MCF-7	breast:
2	chr1:155196978..155198560-chr1:155209319..155211586,2	K562	blood:
3	chr1:155211497..155213419-chr17:60004081..60005775,2	MCF-7	breast:
4	chr1:155214835..155216335-chr17:41464308..41466176,2	K562	blood:
5	chr1:155176876..155179171-chr1:155209871..155213021,3	K562	blood:
6	chr1:155210207..155211789-chr1:155219850..155221900,2	K562	blood:
7	chr1:155209487..155212728-chr1:155212760..155217156,9	MCF-7	breast:
8	chr1:155220311..155221249-chr1:155294702..155295617,4	K562	blood:
9	chr1:155209079..155212795-chr1:155212935..155216540,4	MCF-7	breast:
10	chr1:155209487..155212728-chr1:155212760..155217156,9	MCF-7	breast:
11	chr1:155196821..155197823-chr1:155213854..155215193,5	NB4	blood:
12	chr1:155195600..155203152-chr1:155209955..155216515,9	MCF-7	breast:
13	chr1:150533710..150534533-chr1:155214061..155214778,2	Hela-S3	cervix:
14	chr1:155211806..155213841-chr1:155274140..155275790,2	K562	blood:
15	chr1:155218456..155235751-chr1:155288837..155299195,44	MCF-7	breast:
16	chr1:155213260..155215992-chr1:155291631..155293665,2	K562	blood:
17	chr1:155193188..155195403-chr1:155211959..155214156,2	K562	blood:
18	chr1:155162285..155164607-chr1:155215509..155217658,2	K562	blood:
19	chr1:155220296..155222214-chr1:155276999..155278896,2	K562	blood:
20	chr1:155213102..155215658-chr1:155292526..155295305,4	MCF-7	breast:
21	chr1:155209079..155212795-chr1:155212935..155216540,4	MCF-7	breast:
22	chr1:155220322..155220907-chr1:155474071..155474657,2	MCF-7	breast:
23	chr1:155196524..155199471-chr1:155205933..155208728,2	MCF-7	breast:
24	chr1:155209377..155211075-chr1:155231660..155233982,2	MCF-7	breast:
25	chr1:155212049..155215843-chr1:155293307..155296856,5	MCF-7	breast:
26	chr1:155197109..155197807-chr1:155214053..155214771,4	HCT-116	colon:
27	chr1:155148830..155149338-chr1:155220083..155220748,2	K562	blood:
28	chr1:155214449..155216184-chr1:155237561..155239532,2	MCF-7	breast:
29	chr1:155148838..155149661-chr1:155220174..155220905,2	MCF-7	breast:
30	chr1:155213935..155214771-chr6:26157834..26158708,2	Hela-S3	cervix:
31	chr1:155165258..155167508-chr1:155224721..155226688,2	K562	blood:
32	chr1:155220423..155221123-chr1:155294628..155295130,2	MCF-7	breast:
33	chr1:155021843..155023415-chr1:155222599..155225501,2	MCF-7	breast:
34	chr1:155212781..155214911-chr1:155269991..155272165,2	K562	blood:
35	chr1:155146543..155149271-chr1:155213227..155215655,2	K562	blood:
36	chr1:155176782..155178958-chr1:155221967..155223751,3	K562	blood:
37	chr1:155211622..155214565-chr1:155278095..155280494,4	MCF-7	breast:
38	chr1:155195364..155197876-chr1:155217568..155220600,3	K562	blood:
39	chr1:155163241..155165710-chr1:155212950..155214666,2	MCF-7	breast:
40	chr1:155218380..155223571-chr1:155290636..155294325,6	K562	blood:
41	chr1:155176709..155179007-chr1:155224736..155227425,3	K562	blood:
42	chr1:155207800..155212678-chr1:155214121..155217855,6	K562	blood:
43	chr1:155213885..155214571-chr2:65282830..65283726,2	NB4	blood:
44	chr1:155177038..155178964-chr1:155225105..155226768,2	K562	blood:
45	chr1:155174858..155180302-chr1:155209102..155215747,8	MCF-7	breast:
46	chr1:155210200..155211789-chr1:155219850..155222070,2	K562	blood:
47	chr1:155176435..155177287-chr1:155222687..155223655,2	MCF-7	breast:
48	chr1:155220600..155221175-chr1:155277671..155278619,3	K562	blood:
49	chr1:155217881..155219766-chr1:155287696..155289622,2	K562	blood:
50	chr1:155187157..155191331-chr1:155209670..155212928,5	MCF-7	breast:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SCAMP3	hsa-miR-16-5p	chr1:155226147-155226168
2	FAM189B	hsa-miR-16-5p	chr1:155217412-155217432
3	FAM189B	hsa-miR-16-5p	chr1:155217418-155217412

Variant related genes	Relation type
GBA	TF binding region
FAM189B	TF binding region
ENSG00000216109	TF binding region
GBA	CpG island
FAM189B	CpG island
ENSG00000216109	CpG island
ENSG00000158373	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000160752	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000011523	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000116521	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000236675	chromatin interactions
ENSG00000165359	chromatin interactions
ENSG00000160685	chromatin interactions
ENSG00000203804	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000006757	chromatin interactions
ENSG00000160767	chromatin interactions
ENSG00000108506	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000143627	chromatin interactions
ENSG00000014914	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000152620	chromatin interactions
ENSG00000225235	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000236263	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000223503	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000231064	chromatin interactions

Extended variants
information (count: 851 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370125418	chr1:155207017-155207018	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs72704130	chr1:155207030-155207031	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs570337924	chr1:155207040-155207041	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537631939	chr1:155207047-155207048	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556277010	chr1:155207056-155207057	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189774125	chr1:155207062-155207063	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545478869	chr1:155207072-155207073	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs398123535	chr1:155207143-155207144	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs142662866	chr1:155207144-155207145	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs121908298	chr1:155207148-155207149	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs79696831	chr1:155207160-155207161	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs575127557	chr1:155207180-155207181	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs535896234	chr1:155207190-155207191	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs74731340	chr1:155207202-155207203	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs368425393	chr1:155207209-155207210	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs371856161	chr1:155207213-155207214	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs199628072	chr1:155207214-155207215	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs79215220	chr1:155207217-155207218	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs80116658	chr1:155207220-155207221	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs140955685	chr1:155207229-155207230	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs374117599	chr1:155207230-155207231	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs78973108	chr1:155207244-155207245	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs367968666	chr1:155207249-155207250	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs121908313	chr1:155207261-155207262	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138246400	chr1:155207289-155207290	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs371576958	chr1:155207294-155207295	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs76725886	chr1:155207322-155207323	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs572370038	chr1:155207336-155207337	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546199839	chr1:155207351-155207352	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs74500255	chr1:155207367-155207368	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs121908303	chr1:155207368-155207369	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs140335079	chr1:155207387-155207388	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs368734596	chr1:155207398-155207399	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs372809157	chr1:155207407-155207408	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs377217353	chr1:155207414-155207415	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs367840697	chr1:155207416-155207417	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs562620247	chr1:155207458-155207459	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs529758518	chr1:155207467-155207468	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs555279454	chr1:155207499-155207500	Strong transcription Genic enhancers Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs532811497	chr1:155207521-155207522	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs762488	chr1:155207549-155207550	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs552220439	chr1:155207566-155207567	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2009578	chr1:155207626-155207627	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs111777259	chr1:155207649-155207650	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537692653	chr1:155207681-155207682	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376957951	chr1:155207694-155207695	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549565365	chr1:155207705-155207706	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28678003	chr1:155207733-155207734	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550305278	chr1:155207830-155207831	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535592331	chr1:155207843-155207844	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2485 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155197200-155212800	Weak transcription	Small Intestine	intestine
2	chr1:155198000-155209600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:155198000-155210400	Weak transcription	A549	lung
4	chr1:155198000-155210400	Weak transcription	HMEC	breast
5	chr1:155198000-155210400	Weak transcription	HSMM	muscle
6	chr1:155198000-155210600	Weak transcription	Psoas Muscle	Psoas
7	chr1:155198000-155210800	Weak transcription	Fetal Kidney	kidney
8	chr1:155198200-155207800	Weak transcription	NHLF	lung
9	chr1:155198200-155209600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr1:155198200-155209600	Weak transcription	Fetal Brain Male	brain
11	chr1:155198200-155210400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:155198200-155210400	Weak transcription	Stomach Mucosa	stomach
13	chr1:155198200-155210400	Weak transcription	NHEK	skin
14	chr1:155198200-155210800	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr1:155198200-155210800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:155201200-155210400	Weak transcription	HepG2	liver
17	chr1:155201400-155210400	Weak transcription	K562	blood
18	chr1:155201400-155210600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:155201800-155210400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:155202200-155210400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:155202600-155210400	Weak transcription	Right Atrium	heart
22	chr1:155202800-155210200	Weak transcription	Fetal Lung	lung
23	chr1:155203800-155210400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr1:155204600-155209400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:155204600-155209400	Strong transcription	Spleen	Spleen
26	chr1:155204600-155209600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:155204600-155209600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:155204600-155209800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr1:155204600-155210000	Strong transcription	Fetal Intestine Small	intestine
30	chr1:155204800-155207800	Strong transcription	Esophagus	oesophagus
31	chr1:155204800-155208000	Strong transcription	Stomach Smooth Muscle	stomach
32	chr1:155204800-155208200	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr1:155204800-155208200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:155204800-155209800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr1:155205000-155208000	Strong transcription	Liver	Liver
36	chr1:155205000-155208200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:155205000-155209000	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr1:155205000-155209400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:155205000-155209600	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr1:155205000-155209800	Strong transcription	Adipose Nuclei	Adipose
41	chr1:155205000-155209800	Strong transcription	Thymus	Thymus
42	chr1:155205200-155207600	Strong transcription	Fetal Brain Female	brain
43	chr1:155205200-155208000	Strong transcription	Brain Cingulate Gyrus	brain
44	chr1:155205200-155208200	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr1:155205200-155208200	Strong transcription	Lung	lung
46	chr1:155205200-155208800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr1:155205200-155209400	Strong transcription	Fetal Thymus	thymus
48	chr1:155205400-155207400	Strong transcription	Colonic Mucosa	Colon
49	chr1:155205400-155207400	Strong transcription	Dnd41	blood
50	chr1:155205400-155208000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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