Variant report

Variant	esv34203
Chromosome Location	chr5:95310985-95452324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1505)
CpG islands
(count:366)
Chromatin interactive
region (count:86)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:95359091-95359108	K562	blood:	n/a	n/a
2	ARID3A	chr5:95322539-95323277	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:95351898-95352274	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:95384538-95384656	K562	blood:	n/a	n/a
5	ARID3A	chr5:95353956-95354116	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:95330369-95330382	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:95446244-95446308	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:95450977-95451416	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:95352030-95352315	K562	blood:	n/a	n/a
10	ARID3A	chr5:95312516-95312519	K562	blood:	n/a	n/a
11	ARID3A	chr5:95323723-95325371	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:95336842-95337451	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:95332827-95333432	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:95372942-95373299	HepG2	liver:	n/a	n/a
15	ATF1	chr5:95450456-95450654	K562	blood:	n/a	n/a
16	ATF1	chr5:95353678-95353980	K562	blood:	n/a	n/a
17	ATF1	chr5:95352046-95352289	K562	blood:	n/a	n/a
18	BACH1	chr5:95403879-95404090	K562	blood:	n/a	chr5:95403900-95403914
19	BACH1	chr5:95419522-95419564	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:95332618-95332880	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:95403155-95403208	K562	blood:	n/a	n/a
22	BCL11A	chr5:95419203-95419420	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL3	chr5:95429469-95430215	A549	lung:	n/a	n/a
24	BCLAF1	chr5:95403803-95404304	K562	blood:	n/a	chr5:95403903-95403912
25	BCLAF1	chr5:95403762-95404353	K562	blood:	n/a	chr5:95403903-95403912
26	BHLHE40	chr5:95403758-95403763	K562	blood:	n/a	n/a
27	BHLHE40	chr5:95416311-95416524	K562	blood:	n/a	n/a
28	BHLHE40	chr5:95322641-95323582	HepG2	liver:	n/a	n/a
29	BHLHE40	chr5:95351971-95352249	K562	blood:	n/a	n/a
30	BHLHE40	chr5:95414995-95415053	K562	blood:	n/a	n/a
31	BHLHE40	chr5:95384654-95384708	K562	blood:	n/a	n/a
32	BRCA1	chr5:95403730-95404260	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr5:95429596-95430220	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:95414824-95415041	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr5:95353672-95353988	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr5:95429582-95430336	HCT-116	colon:	n/a	n/a
37	CBX3	chr5:95373344-95373712	K562	blood:	n/a	n/a
38	CBX3	chr5:95414735-95415297	HCT-116	colon:	n/a	n/a
39	CBX3	chr5:95340459-95340835	K562	blood:	n/a	n/a
40	CBX3	chr5:95403471-95404286	HCT-116	colon:	n/a	n/a
41	CBX3	chr5:95340512-95340786	K562	blood:	n/a	n/a
42	CCNT2	chr5:95323509-95323560	K562	blood:	n/a	n/a
43	CCNT2	chr5:95403725-95404183	K562	blood:	n/a	n/a
44	CCNT2	chr5:95352071-95352262	K562	blood:	n/a	chr5:95352194-95352214
45	CCNT2	chr5:95353748-95353935	K562	blood:	n/a	n/a
46	CEBPB	chr5:95385139-95385463	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:95384425-95384748	K562	blood:	n/a	n/a
48	CEBPB	chr5:95429885-95430125	A549	lung:	n/a	chr5:95429974-95429986
49	CEBPB	chr5:95406343-95406589	K562	blood:	n/a	n/a
50	CEBPB	chr5:95430558-95430957	ECC-1	luminal epithelium:	n/a	chr5:95430783-95430794

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:95413871-95413921	HMEC	breast:	n/a
2	chr5:95361197-95361247	NHBE	bronchial:	n/a
3	chr5:95419503-95419553	HCF	heart:	n/a
4	chr5:95419503-95419553	NHBE	bronchial:	n/a
5	chr5:95321963-95322013	SK-N-MC	brain:	n/a
6	chr5:95413871-95413921	AG09309	skin:	n/a
7	chr5:95361197-95361247	HepG2	liver:	n/a
8	chr5:95413871-95413921	HCM	heart:	n/a
9	chr5:95361197-95361247	HCM	heart:	n/a
10	chr5:95321963-95322013	NHBE	bronchial:	n/a
11	chr5:95409135-95409185	HMEC	breast:	n/a
12	chr5:95419503-95419553	HEK293	kidney:	embryo
13	chr5:95321963-95322013	PFSK-1	brain:	n/a
14	chr5:95321963-95322013	PANC-1	pancreas:	n/a
15	chr5:95413871-95413921	HRE	kidney:	n/a
16	chr5:95361197-95361247	HMEC	breast:	n/a
17	chr5:95321963-95322013	HAEpiC	amniotic membrane:	n/a
18	chr5:95361197-95361247	ProgFib	skin:	n/a
19	chr5:95413861-95413911	H1-hESC	embryonic stem cell:	embryo
20	chr5:95419503-95419553	Caco-2	colon:	n/a
21	chr5:95413861-95413911	Hepatocyte	liver:	n/a
22	chr5:95413861-95413911	HAEpiC	amniotic membrane:	n/a
23	chr5:95409135-95409185	AG10803	skin:	n/a
24	chr5:95321963-95322013	HEK293	kidney:	embryo
25	chr5:95419503-95419553	MCF10A-Er-Src	breast:	n/a
26	chr5:95321963-95322013	HCM	heart:	n/a
27	chr5:95419503-95419553	GM12892	blood:	n/a
28	chr5:95413871-95413921	AG09319	gingival:	n/a
29	chr5:95419503-95419553	PANC-1	pancreas:	n/a
30	chr5:95413861-95413911	ovcar-3	ovarian:	n/a
31	chr5:95321963-95322013	GM19239	blood:	n/a
32	chr5:95419503-95419553	SKMC	muscle:	n/a
33	chr5:95321963-95322013	AG09319	gingival:	n/a
34	chr5:95321963-95322013	GM12892	blood:	n/a
35	chr5:95321963-95322013	T-47D	breast:	n/a
36	chr5:95321963-95322013	K562	blood:	n/a
37	chr5:95413871-95413921	NHDF-neo	bronchial:	n/a
38	chr5:95409135-95409185	NT2-D1	testis:	n/a
39	chr5:95413871-95413921	HCF	heart:	n/a
40	chr5:95419503-95419553	SK-N-MC	brain:	n/a
41	chr5:95321963-95322013	AG09309	skin:	n/a
42	chr5:95413871-95413921	HepG2	liver:	n/a
43	chr5:95413871-95413921	MCF-7	breast:	n/a
44	chr5:95409135-95409185	IMR90	lung:	fetal
45	chr5:95409135-95409185	NHBE	bronchial:	n/a
46	chr5:95413871-95413921	SAEC	small airway:	n/a
47	chr5:95321963-95322013	HCF	heart:	n/a
48	chr5:95413871-95413921	BE2_C	brain:	n/a
49	chr5:95361197-95361247	ECC-1	luminal epithelium:	n/a
50	chr5:95409135-95409185	MCF-7	breast:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:95296314..95298555-chr5:95397660..95400268,2	K562	blood:
2	chr5:95362269..95364371-chr5:95402115..95403817,2	K562	blood:
3	chr5:95297972..95300750-chr5:95328029..95330073,2	K562	blood:
4	chr5:95363683..95365395-chr5:95366901..95369484,2	K562	blood:
5	chr11:64013141..64015957-chr5:95386899..95388399,2	MCF-7	breast:
6	chr5:95402259..95403987-chr5:95413723..95416198,2	K562	blood:
7	chr5:95416575..95419199-chr5:95425271..95427989,2	K562	blood:
8	chr5:95296442..95299221-chr5:95402366..95405358,3	K562	blood:
9	chr5:95322876..95325746-chr5:95335508..95338099,2	K562	blood:
10	chr5:95351011..95353911-chr5:95402617..95404215,2	K562	blood:
11	chr5:95448479..95450941-chr5:95454659..95457285,2	MCF-7	breast:
12	chr5:95394397..95397979-chr5:95402204..95405493,4	K562	blood:
13	chr5:95395858..95398808-chr5:95403139..95405435,2	K562	blood:
14	chr5:95351011..95353911-chr5:95402617..95404215,2	K562	blood:
15	chr5:95295655..95298675-chr5:95421963..95424725,3	MCF-7	breast:
16	chr5:95304291..95306265-chr5:95309546..95312179,2	K562	blood:
17	chr5:95334613..95336349-chr5:95402257..95404926,2	K562	blood:
18	chr5:95295987..95299495-chr5:95427071..95430521,5	MCF-7	breast:
19	chr5:95408446..95411161-chr5:95411273..95412980,2	K562	blood:
20	chr5:95363683..95365395-chr5:95366901..95369484,2	K562	blood:
21	chr5:95328505..95331232-chr5:95332077..95333739,2	K562	blood:
22	chr5:95372818..95374675-chr5:95378795..95380652,2	MCF-7	breast:
23	chr5:95309496..95312774-chr5:95317440..95321403,4	K562	blood:
24	chr5:95322876..95325746-chr5:95335508..95338099,2	K562	blood:
25	chr5:95445238..95446778-chr5:95449413..95451842,2	K562	blood:
26	chr5:95406044..95407989-chr5:95410489..95412810,2	K562	blood:
27	chr5:95331250..95333197-chr5:95339157..95340673,2	K562	blood:
28	chr5:95359766..95362858-chr5:95371780..95373834,3	MCF-7	breast:
29	chr5:95296910..95298799-chr5:95356285..95359042,2	K562	blood:
30	chr5:95192803..95195845-chr5:95402156..95405628,4	K562	blood:
31	chr5:95315592..95318103-chr5:95322606..95324931,2	K562	blood:
32	chr5:95327677..95330005-chr5:95332077..95333718,2	K562	blood:
33	chr5:95296782..95299195-chr5:95402497..95405358,3	K562	blood:
34	chr5:95399534..95401780-chr5:95407826..95410205,2	K562	blood:
35	chr5:95194068..95196070-chr5:95401310..95403656,2	K562	blood:
36	chr5:95362269..95364371-chr5:95402115..95403817,2	K562	blood:
37	chr5:95445238..95446778-chr5:95449413..95451842,2	K562	blood:
38	chr5:95359766..95362858-chr5:95371780..95373834,3	MCF-7	breast:
39	chr5:95294090..95296695-chr5:95356956..95358736,2	K562	blood:
40	chr5:95330891..95333849-chr5:95334417..95336264,2	K562	blood:
41	chr5:95360554..95363561-chr5:95366063..95368612,3	K562	blood:
42	chr5:95262626..95265334-chr5:95402014..95404790,2	K562	blood:
43	chr5:95408446..95411161-chr5:95411273..95412980,2	K562	blood:
44	chr5:95363657..95366374-chr5:95368522..95371027,2	MCF-7	breast:
45	chr5:95401885..95403759-chr5:95409386..95411340,2	K562	blood:
46	chr5:95398261..95399913-chr5:95401508..95403607,2	K562	blood:
47	chr5:95330891..95333849-chr5:95334417..95336264,2	K562	blood:
48	chr5:95390171..95391884-chr5:95392902..95395243,2	K562	blood:
49	chr5:95408738..95411394-chr5:95414154..95415888,2	MCF-7	breast:
50	chr5:95401885..95403759-chr5:95409386..95411340,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELL2-2	chr5:95338604-95339260	NONHSAT102881
2	lnc-ELL2-1	chr5:95316041-95316231	ENSG00000250955.1
3	lnc-ELL2-1	chr5:95321964-95322015	ENSG00000250955.1
4	lnc-C5orf27-3	chr5:95385819-95385905	ENSG00000250551
5	lnc-C5orf27-3	chr5:95446638-95446709	ENSG00000250551

miRNA name	Chromosome Location	mirBase accession
hsa-miR-583	chr5:95414857-95414877	MIMAT0003248

No data

Variant related genes	Relation type
FABP5P5	TF binding region
MIR583	TF binding region
ENSG00000250955	TF binding region
ENSG00000250551	TF binding region
FABP5P5	CpG island
MIR583	CpG island
ENSG00000250955	CpG island
ENSG00000250551	CpG island
ENSG00000250551	chromatin interactions
ENSG00000173457	chromatin interactions
ENSG00000207578	chromatin interactions
ENSG00000256940	chromatin interactions
ENSG00000251314	chromatin interactions
ENSG00000118985	chromatin interactions
ENSG00000250955	chromatin interactions

Extended variants
information (count: 4537 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4537 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10515232	chr5:95310985-95310986	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148849636	chr5:95311065-95311066	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs143519075	chr5:95311086-95311087	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs77836323	chr5:95311159-95311160	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs17085371	chr5:95311171-95311172	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs17085373	chr5:95311203-95311204	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183911168	chr5:95311233-95311234	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs73771830	chr5:95311244-95311245	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs554909239	chr5:95311270-95311271	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs532182463	chr5:95311283-95311284	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs189969337	chr5:95311294-95311295	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs181720665	chr5:95311361-95311362	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548033854	chr5:95311421-95311422	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557621402	chr5:95311452-95311453	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs17085377	chr5:95311519-95311520	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546377495	chr5:95311532-95311533	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs6861075	chr5:95311548-95311549	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs17085383	chr5:95311580-95311581	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs573338828	chr5:95311585-95311586	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs116691105	chr5:95311606-95311607	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562091082	chr5:95311616-95311617	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530916122	chr5:95311628-95311629	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs148010258	chr5:95311674-95311675	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs568573744	chr5:95311686-95311687	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs113461761	chr5:95311855-95311856	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs547930248	chr5:95311856-95311857	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs546732477	chr5:95311865-95311866	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs141914152	chr5:95311915-95311916	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs533819495	chr5:95312008-95312009	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs535150884	chr5:95312029-95312030	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs374047692	chr5:95312035-95312036	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs145792053	chr5:95312057-95312058	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs187147554	chr5:95312118-95312119	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs553369289	chr5:95312142-95312143	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs367588943	chr5:95312148-95312149	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138895350	chr5:95312168-95312169	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs6888205	chr5:95312254-95312255	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577421862	chr5:95312303-95312304	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs539657190	chr5:95312317-95312318	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs34434273	chr5:95312397-95312398	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553573648	chr5:95312450-95312451	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs573450513	chr5:95312475-95312476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190232039	chr5:95312570-95312571	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs77843162	chr5:95312571-95312572	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150766323	chr5:95312577-95312578	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544547994	chr5:95312677-95312678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138060190	chr5:95312682-95312683	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs10515233	chr5:95312717-95312718	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs115233453	chr5:95312728-95312729	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559202756	chr5:95312752-95312753	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1520 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95298800-95322600	Weak transcription	Pancreas	Pancrea
2	chr5:95307400-95318800	Weak transcription	HepG2	liver
3	chr5:95308800-95311800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr5:95309000-95311000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr5:95309000-95312000	Enhancers	K562	blood
6	chr5:95309400-95311800	Enhancers	Dnd41	blood
7	chr5:95309600-95311200	Enhancers	Fetal Lung	lung
8	chr5:95309600-95314200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr5:95309800-95311000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:95310400-95312800	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr5:95310600-95312200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr5:95310800-95312400	Weak transcription	HSMM	muscle
13	chr5:95311200-95312600	Weak transcription	Fetal Lung	lung
14	chr5:95311600-95311800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr5:95311800-95316600	Weak transcription	Dnd41	blood
16	chr5:95312400-95313000	Enhancers	HSMM	muscle
17	chr5:95312600-95312800	Enhancers	Fetal Lung	lung
18	chr5:95312600-95313200	Enhancers	NHDF-Ad	bronchial
19	chr5:95312800-95313000	Enhancers	Muscle Satellite Cultured Cells	--
20	chr5:95313000-95319800	Weak transcription	HSMM	muscle
21	chr5:95314200-95315000	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr5:95315000-95319600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr5:95315200-95317800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr5:95316400-95316800	Weak transcription	Aorta	Aorta
25	chr5:95316400-95316800	Active TSS	Gastric	stomach
26	chr5:95316600-95317200	Enhancers	Dnd41	blood
27	chr5:95316800-95317200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr5:95316800-95324000	Weak transcription	Gastric	stomach
29	chr5:95318000-95319000	Enhancers	Fetal Heart	heart
30	chr5:95318000-95320800	Weak transcription	Colon Smooth Muscle	Colon
31	chr5:95318200-95318400	Enhancers	Fetal Intestine Large	intestine
32	chr5:95318200-95325000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr5:95318200-95327600	Enhancers	Fetal Intestine Small	intestine
34	chr5:95318600-95320000	Weak transcription	Fetal Intestine Large	intestine
35	chr5:95318800-95322600	Enhancers	HepG2	liver
36	chr5:95318800-95323000	Enhancers	Liver	Liver
37	chr5:95319000-95321600	Weak transcription	Fetal Heart	heart
38	chr5:95319000-95322200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:95319600-95320000	Enhancers	A549	lung
40	chr5:95319600-95320200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:95319600-95320200	Enhancers	Hela-S3	cervix
42	chr5:95319600-95320400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr5:95319600-95320800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:95319600-95322200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr5:95319600-95325600	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr5:95319800-95320000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:95319800-95320400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr5:95319800-95320400	Enhancers	NHLF	lung
49	chr5:95319800-95320600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr5:95319800-95320600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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