Variant report

Variant	esv3325021
Chromosome Location	chr1:212002754-212005502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:855)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:212002717-212003060	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:212004061-212004297	K562	blood:	n/a	n/a
3	ATF3	chr1:212003867-212004218	K562	blood:	n/a	n/a
4	BACH1	chr1:212002956-212003106	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:212003904-212004096	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:212003322-212003364	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr1:212003820-212004640	GM12878	blood:	n/a	chr1:212004187-212004200 chr1:212004114-212004123 chr1:212004148-212004157 chr1:212004191-212004204 chr1:212004187-212004196 chr1:212004184-212004193 chr1:212004165-212004173
8	BCLAF1	chr1:212003244-212003693	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:212003701-212003833	K562	blood:	n/a	n/a
10	BHLHE40	chr1:212004001-212004250	GM12878	blood:	n/a	chr1:212004184-212004200 chr1:212004190-212004206
11	BHLHE40	chr1:212004078-212004485	K562	blood:	n/a	chr1:212004184-212004200 chr1:212004190-212004206
12	BRCA1	chr1:212004347-212004418	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:212004261-212004432	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:212003946-212004374	K562	blood:	n/a	n/a
15	CCNT2	chr1:212003321-212004415	K562	blood:	n/a	chr1:212004229-212004238
16	CEBPB	chr1:212002704-212003108	K562	blood:	n/a	n/a
17	CEBPB	chr1:212002781-212002953	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:212002700-212003078	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:212002559-212003165	A549	lung:	n/a	n/a
20	CEBPB	chr1:212002711-212003077	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:212002567-212003044	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:212002756-212002974	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:212002692-212003085	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:212004030-212004327	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:212002694-212003457	A549	lung:	n/a	n/a
26	CEBPB	chr1:212002650-212003100	K562	blood:	n/a	n/a
27	CEBPB	chr1:212002660-212003031	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:212002643-212003091	A549	lung:	n/a	n/a
29	CEBPB	chr1:212002711-212002973	K562	blood:	n/a	n/a
30	CEBPB	chr1:212002694-212003061	MCF-7	breast:	n/a	n/a
31	CEBPB	chr1:212003290-212003583	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:212003343-212003440	K562	blood:	n/a	n/a
33	CEBPD	chr1:212003781-212004208	HepG2	liver:	n/a	n/a
34	CHD1	chr1:212004037-212004517	GM12878	blood:	n/a	n/a
35	CHD1	chr1:212002968-212003440	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr1:212003223-212003716	GM12878	blood:	n/a	n/a
37	CHD1	chr1:212003867-212004015	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:212004012-212004503	GM12878	blood:	n/a	n/a
39	CHD2	chr1:212004142-212004549	HepG2	liver:	n/a	n/a
40	CHD2	chr1:212004131-212004346	K562	blood:	n/a	n/a
41	CHD2	chr1:212003239-212004425	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr1:212003628-212003662	K562	blood:	n/a	n/a
43	CHD2	chr1:212003714-212003914	HepG2	liver:	n/a	n/a
44	CHD2	chr1:212004172-212004205	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr1:212003536-212004393	A549	lung:	n/a	n/a
46	CTCF	chr1:212004120-212004270	HCT-116	colon:	n/a	chr1:212004161-212004182 chr1:212004167-212004183
47	CTCF	chr1:212004380-212004530	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:212004100-212004250	GM12878	blood:	n/a	chr1:212004161-212004182 chr1:212004167-212004183
49	CTCF	chr1:212002700-212002850	HRE	kidney:	n/a	n/a
50	CTCF	chr1:212002680-212002830	HA-sp	spinal cord:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:212004782-212004832	Jurkat	blood:	n/a
2	chr1:212004782-212004832	Jurkat	blood:	n/a
3	chr1:212004782-212004832	AG04449	skin:	fetal
4	chr1:212003989-212004039	GM06990	blood:	n/a
5	chr1:212003989-212004039	T-47D	breast:	n/a
6	chr1:212003977-212004027	BE2_C	brain:	n/a
7	chr1:212003989-212004039	AoSMC	blood vessel:	n/a
8	chr1:212004261-212004311	BE2_C	brain:	n/a
9	chr1:212003502-212003552	HRPEpiC	eye:	n/a
10	chr1:212003502-212003552	HIPEpiC	eye:	n/a
11	chr1:212003961-212004011	SK-N-SH	brain:	n/a
12	chr1:212003989-212004039	PANC-1	pancreas:	n/a
13	chr1:212004408-212004458	GM12878	blood:	n/a
14	chr1:212003961-212004011	ECC-1	luminal epithelium:	n/a
15	chr1:212004275-212004325	HCF	heart:	n/a
16	chr1:212004275-212004325	AG09319	gingival:	n/a
17	chr1:212004408-212004458	LNCaP	prostate:	n/a
18	chr1:212003977-212004027	HUVEC	blood vessel:	n/a
19	chr1:212004408-212004458	HCPEpiC	choroid plexus:	n/a
20	chr1:212004169-212004219	SKMC	muscle:	n/a
21	chr1:212004275-212004325	BE2_C	brain:	n/a
22	chr1:212003961-212004011	HNPCEpiC	eye:	n/a
23	chr1:212003961-212004011	HRE	kidney:	n/a
24	chr1:212004261-212004311	CMK	blood:	n/a
25	chr1:212002970-212003020	NB4	blood:	n/a
26	chr1:212003502-212003552	K562	blood:	n/a
27	chr1:212004261-212004311	HUVEC	blood vessel:	n/a
28	chr1:212003502-212003552	SK-N-SH	brain:	n/a
29	chr1:212004408-212004458	ProgFib	skin:	n/a
30	chr1:212004782-212004832	IMR90	lung:	fetal
31	chr1:212002970-212003020	HCF	heart:	n/a
32	chr1:212002970-212003020	HEK293	kidney:	embryo
33	chr1:212004169-212004219	ECC-1	luminal epithelium:	n/a
34	chr1:212004327-212004377	Caco-2	colon:	n/a
35	chr1:212002770-212002820	SK-N-SH	brain:	n/a
36	chr1:212004408-212004458	PrEC	prostate:	n/a
37	chr1:212003502-212003552	NHDF-neo	bronchial:	n/a
38	chr1:212004782-212004832	GM12892	blood:	n/a
39	chr1:212004169-212004219	GM12891	blood:	n/a
40	chr1:212004275-212004325	SK-N-SH	brain:	n/a
41	chr1:212004169-212004219	NT2-D1	testis:	n/a
42	chr1:212004782-212004832	HIPEpiC	eye:	n/a
43	chr1:212003961-212004011	NB4	blood:	n/a
44	chr1:212004327-212004377	NH-A	brain:	n/a
45	chr1:212004261-212004311	GM12891	blood:	n/a
46	chr1:212004408-212004458	AG04449	skin:	fetal
47	chr1:212004782-212004832	RPTEC	kidney:	n/a
48	chr1:212002770-212002820	HCF	heart:	n/a
49	chr1:212004261-212004311	GM06990	blood:	n/a
50	chr1:212004169-212004219	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:211873619..211875227-chr1:212000952..212002871,2	K562	blood:
2	chr1:212002304..212005337-chr1:212206926..212210304,4	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTL-2	chr1:212004303-212004382	ENSG00000229258.1
2	lnc-DTL-2	chr1:212004552-212004754	NONHSAT009333
3	lnc-DTL-2	chr1:212004587-212004754	ENSG00000229258.1
4	lnc-DTL-2	chr1:212004303-212004382	NONHSAT009333
5	lnc-DTL-2	chr1:212003188-212003260	ENSG00000229258.1
6	lnc-DTL-2	chr1:212004689-212004754	ENSG00000229258.1
7	lnc-DTL-2	chr1:212004598-212004754	ENSG00000229258.1
8	lnc-DTL-2	chr1:212004690-212004754	ENSG00000229258.1

No data

Variant related genes	Relation type
ENSG00000229258	TF binding region
LPGAT1	TF binding region
ENSG00000229258	CpG island
LPGAT1	CpG island
ENSG00000143476	chromatin interactions
ENSG00000143493	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189767866	chr1:212002766-212002767	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs151259797	chr1:212002789-212002790	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs548935522	chr1:212002791-212002792	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs140498655	chr1:212002795-212002796	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs78187247	chr1:212002807-212002808	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs552151642	chr1:212002818-212002819	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs182110737	chr1:212002858-212002859	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs537962110	chr1:212002937-212002938	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs187019313	chr1:212002946-212002947	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs191504945	chr1:212002965-212002966	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs183231794	chr1:212002972-212002973	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs563567356	chr1:212002979-212002980	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs553790260	chr1:212002983-212002984	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs145615452	chr1:212003039-212003040	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs552129248	chr1:212003050-212003051	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs138321387	chr1:212003087-212003088	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs545739342	chr1:212003119-212003120	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs375080088	chr1:212003198-212003199	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs5780661	chr1:212003211-212003212	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs33961821	chr1:212003212-212003213	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs545926529	chr1:212003215-212003216	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs564256157	chr1:212003219-212003220	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs397982804	chr1:212003221-212003222	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs201891168	chr1:212003222-212003223	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs200091356	chr1:212003224-212003225	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs372838994	chr1:212003245-212003246	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs558926479	chr1:212003261-212003262	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs577143748	chr1:212003286-212003287	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs7549142	chr1:212003307-212003308	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562957438	chr1:212003315-212003316	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528187096	chr1:212003358-212003359	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530360252	chr1:212003362-212003363	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs371833380	chr1:212003377-212003378	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs542438014	chr1:212003387-212003388	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142832019	chr1:212003391-212003392	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs368165715	chr1:212003423-212003424	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs568163762	chr1:212003425-212003426	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs78376285	chr1:212003491-212003492	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs527994482	chr1:212003559-212003560	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113129902	chr1:212003589-212003590	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs552557989	chr1:212003611-212003612	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs570449965	chr1:212003651-212003652	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs150144350	chr1:212003675-212003676	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs368753113	chr1:212003771-212003772	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs567813463	chr1:212003827-212003828	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs369237609	chr1:212003846-212003847	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs537599183	chr1:212003865-212003866	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs113456517	chr1:212003917-212003918	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs562759380	chr1:212004011-212004012	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs547199971	chr1:212004040-212004041	Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	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
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211952200-212003000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:211986200-212002800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:211989600-212002800	Weak transcription	Lung	lung
4	chr1:211995000-212002800	Weak transcription	Fetal Lung	lung
5	chr1:211997800-212003000	Weak transcription	Esophagus	oesophagus
6	chr1:211997800-212003000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:211999400-212002800	Active TSS	GM12878-XiMat	blood
8	chr1:211999400-212004400	Active TSS	Fetal Intestine Small	intestine
9	chr1:212000200-212004600	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr1:212000600-212002800	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr1:212000800-212003000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:212000800-212003200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr1:212000800-212003400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr1:212000800-212004400	Active TSS	Brain Hippocampus Middle	brain
15	chr1:212001000-212002800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:212001000-212002800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr1:212001200-212004600	Active TSS	Brain Cingulate Gyrus	brain
18	chr1:212001200-212004800	Active TSS	Brain Angular Gyrus	brain
19	chr1:212001400-212002800	Enhancers	Primary B cells from peripheral blood	blood
20	chr1:212001400-212003000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr1:212001600-212002800	Weak transcription	Gastric	stomach
22	chr1:212001600-212003000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr1:212001600-212004400	Active TSS	Brain Substantia Nigra	brain
24	chr1:212001600-212004600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr1:212002000-212004600	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr1:212002000-212004800	Active TSS	Right Atrium	heart
27	chr1:212002200-212003000	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr1:212002200-212003000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr1:212002200-212003200	Flanking Active TSS	Fetal Brain Male	brain
30	chr1:212002200-212003400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:212002200-212003400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr1:212002400-212002800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:212002400-212002800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr1:212002400-212002800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:212002400-212002800	Weak transcription	Primary T cells from cord blood	blood
36	chr1:212002400-212002800	Flanking Active TSS	Brain Germinal Matrix	brain
37	chr1:212002400-212002800	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr1:212002400-212002800	Enhancers	Small Intestine	intestine
39	chr1:212002400-212002800	Enhancers	Stomach Mucosa	stomach
40	chr1:212002400-212002800	Flanking Active TSS	HepG2	liver
41	chr1:212002400-212002800	Flanking Active TSS	NH-A	brain
42	chr1:212002400-212002800	Flanking Active TSS	NHDF-Ad	bronchial
43	chr1:212002400-212002800	Enhancers	NHEK	skin
44	chr1:212002400-212002800	Active TSS	Osteobl	bone
45	chr1:212002400-212003000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
46	chr1:212002400-212003000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
47	chr1:212002400-212003000	Enhancers	Primary T cells fromperipheralblood	blood
48	chr1:212002400-212003000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr1:212002400-212003000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:212002400-212003000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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