Variant report

Variant	nsv889549
Chromosome Location	chr7:153627177-153682815
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:153631881-153631909	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:153671731-153672005	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:153631179-153631191	HepG2	liver:	n/a	n/a
4	CEBPB	chr7:153632851-153633134	HepG2	liver:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
5	CEBPB	chr7:153653827-153654031	K562	blood:	n/a	chr7:153653924-153653933
6	CEBPB	chr7:153661713-153661899	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:153671722-153671982	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:153653846-153654075	A549	lung:	n/a	chr7:153653924-153653933
9	CEBPB	chr7:153650331-153650429	K562	blood:	n/a	n/a
10	CEBPB	chr7:153636771-153636970	K562	blood:	n/a	n/a
11	CEBPB	chr7:153649215-153649575	A549	lung:	n/a	chr7:153649388-153649399
12	CEBPB	chr7:153632890-153633162	K562	blood:	n/a	chr7:153632987-153632998 chr7:153632987-153633000
13	CEBPB	chr7:153649223-153649552	HepG2	liver:	n/a	chr7:153649388-153649399
14	CHD2	chr7:153653758-153653916	HepG2	liver:	n/a	n/a
15	CTCF	chr7:153636960-153637110	AG04449	skin:	n/a	n/a
16	CTCF	chr7:153655901-153655912	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr7:153645250-153645405	LNCaP	prostate:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
18	CTCF	chr7:153645240-153645390	SK-N-SH_RA	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
19	CTCF	chr7:153645141-153645515	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
20	CTCF	chr7:153668897-153668985	GM20000	blood:	n/a	n/a
21	CTCF	chr7:153645320-153645470	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
22	CTCF	chr7:153645260-153645410	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
23	CTCF	chr7:153645257-153645434	LNCaP	prostate:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
24	CTCF	chr7:153645243-153645423	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
25	CTCF	chr7:153645332-153645347	Hela-S3	cervix:	n/a	chr7:153645332-153645340
26	CTCF	chr7:153645260-153645410	A549	lung:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
27	CTCF	chr7:153645260-153645410	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
28	CTCF	chr7:153645206-153645506	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
29	CTCF	chr7:153645254-153645428	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
30	CTCF	chr7:153645255-153645431	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
31	CTCF	chr7:153659757-153659816	LNCaP	prostate:	n/a	n/a
32	CTCF	chr7:153645108-153645544	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
33	CTCF	chr7:153645248-153645411	Medullo	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
34	CTCF	chr7:153645220-153645370	SK-N-SH_RA	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
35	CTCF	chr7:153645140-153645290	A549	lung:	n/a	n/a
36	CTCF	chr7:153645200-153645350	Caco-2	colon:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340
37	CTCF	chr7:153645200-153645350	WERI-Rb-1	eye:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340
38	CTCF	chr7:153631322-153631410	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:153645280-153645430	K562	blood:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
40	CTCF	chr7:153645280-153645411	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
41	CTCF	chr7:153672056-153672078	GM20000	blood:	n/a	n/a
42	CTCF	chr7:153643759-153643799	GM20000	blood:	n/a	n/a
43	CTCF	chr7:153645240-153645390	HRE	kidney:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
44	CTCF	chr7:153657784-153657790	GM19239	blood:	n/a	n/a
45	CTCF	chr7:153645153-153645562	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
46	CTCF	chr7:153645220-153645370	HEK293	kidney:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
47	CTCF	chr7:153645280-153645430	BE2_C	brain:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
48	CTCF	chr7:153645240-153645390	MCF-7	breast:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352
49	CTCF	chr7:153680841-153680918	Fibrobl	skin:	n/a	n/a
50	CTCF	chr7:153645272-153645418	HepG2	liver:	n/a	chr7:153645329-153645347 chr7:153645330-153645346 chr7:153645332-153645340 chr7:153645331-153645352

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153641267-153641317	CMK	blood:	n/a
2	chr7:153641242-153641292	GM12878	blood:	n/a
3	chr7:153641307-153641357	T-47D	breast:	n/a
4	chr7:153641267-153641317	AG10803	skin:	n/a
5	chr7:153641242-153641292	H1-hESC	embryonic stem cell:	embryo
6	chr7:153641307-153641357	RPTEC	kidney:	n/a
7	chr7:153641267-153641317	SK-N-SH_RA	brain:	n/a
8	chr7:153641307-153641357	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:153641307-153641357	HRE	kidney:	n/a
10	chr7:153641307-153641357	HIPEpiC	eye:	n/a
11	chr7:153641307-153641357	SK-N-SH	brain:	n/a
12	chr7:153641307-153641357	BE2_C	brain:	n/a
13	chr7:153641307-153641357	NT2-D1	testis:	n/a
14	chr7:153641307-153641357	HCF	heart:	n/a
15	chr7:153641242-153641292	AG10803	skin:	n/a
16	chr7:153641267-153641317	K562	blood:	n/a
17	chr7:153641267-153641317	MCF10A-Er-Src	breast:	n/a
18	chr7:153641267-153641317	ECC-1	luminal epithelium:	n/a
19	chr7:153641307-153641357	HCPEpiC	choroid plexus:	n/a
20	chr7:153641307-153641357	NB4	blood:	n/a
21	chr7:153641242-153641292	HRCEpiC	kidney:	n/a
22	chr7:153641267-153641317	SK-N-SH	brain:	n/a
23	chr7:153641242-153641292	GM19239	blood:	n/a
24	chr7:153641267-153641317	HRPEpiC	eye:	n/a
25	chr7:153641242-153641292	T-47D	breast:	n/a
26	chr7:153641307-153641357	BJ	skin:	n/a
27	chr7:153641242-153641292	ProgFib	skin:	n/a
28	chr7:153641267-153641317	GM12892	blood:	n/a
29	chr7:153641307-153641357	A549	lung:	n/a
30	chr7:153641267-153641317	Hepatocyte	liver:	n/a
31	chr7:153641307-153641357	GM12892	blood:	n/a
32	chr7:153641267-153641317	GM06990	blood:	n/a
33	chr7:153641242-153641292	Hepatocyte	liver:	n/a
34	chr7:153641267-153641317	HEEpiC	esophagus:	n/a
35	chr7:153641267-153641317	Jurkat	blood:	n/a
36	chr7:153641307-153641357	AG04449	skin:	fetal
37	chr7:153641242-153641292	HepG2	liver:	n/a
38	chr7:153641267-153641317	SKMC	muscle:	n/a
39	chr7:153641242-153641292	U87	brain:	n/a
40	chr7:153641307-153641357	HMEC	breast:	n/a
41	chr7:153641267-153641317	GM19239	blood:	n/a
42	chr7:153641267-153641317	NHDF-neo	bronchial:	n/a
43	chr7:153641267-153641317	NHBE	bronchial:	n/a
44	chr7:153641267-153641317	AG09309	skin:	n/a
45	chr7:153641242-153641292	SK-N-MC	brain:	n/a
46	chr7:153641307-153641357	SAEC	small airway:	n/a
47	chr7:153641242-153641292	PrEC	prostate:	n/a
48	chr7:153641307-153641357	Caco-2	colon:	n/a
49	chr7:153641307-153641357	HCM	heart:	n/a
50	chr7:153641267-153641317	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:153636379..153638876-chr7:153641967..153644697,4	K562	blood:
2	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
3	chr7:153104450..153106704-chr7:153631945..153634979,3	K562	blood:
4	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:
5	chr7:153646257..153648420-chr7:153652652..153654403,2	K562	blood:
6	chr7:153646257..153648420-chr7:153652652..153654403,2	K562	blood:
7	chr7:153636379..153638876-chr7:153641967..153644697,4	K562	blood:
8	chr7:153630679..153632497-chr7:153633918..153635661,2	K562	blood:
9	chr7:153636605..153638915-chr7:153643180..153645983,3	K562	blood:

Variant related genes	Relation type
ENSG00000226509	TF binding region
ENSG00000226509	CpG island

Extended variants
information (count: 1315 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1315 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543274806	chr7:153627280-153627281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182246576	chr7:153627341-153627342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571372022	chr7:153627421-153627422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531388312	chr7:153627503-153627504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376252184	chr7:153627504-153627505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370594648	chr7:153627526-153627527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs71545656	chr7:153627539-153627540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115081722	chr7:153627572-153627573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538881368	chr7:153627586-153627587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554329492	chr7:153627625-153627626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374619416	chr7:153627704-153627705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562563070	chr7:153627731-153627732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533021440	chr7:153627732-153627733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551402310	chr7:153627748-153627749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146351854	chr7:153627792-153627793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184956556	chr7:153627829-153627830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116702249	chr7:153627882-153627883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567378576	chr7:153628016-153628017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538040166	chr7:153628098-153628099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34470834	chr7:153628168-153628169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190208563	chr7:153628306-153628307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56960776	chr7:153628416-153628417	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538700611	chr7:153628426-153628427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374930180	chr7:153628436-153628437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572368241	chr7:153628441-153628442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546234404	chr7:153628445-153628446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555220053	chr7:153628468-153628469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11769195	chr7:153628469-153628470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10262888	chr7:153628523-153628524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17173836	chr7:153628576-153628577	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs565435096	chr7:153628586-153628587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11437921	chr7:153628654-153628655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397945723	chr7:153628661-153628662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533085673	chr7:153628691-153628692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17173837	chr7:153628692-153628693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560226045	chr7:153628724-153628725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183195914	chr7:153628735-153628736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549055335	chr7:153628738-153628739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188533881	chr7:153628768-153628769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531464594	chr7:153628871-153628872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373792293	chr7:153628883-153628884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117632789	chr7:153628946-153628947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538760569	chr7:153628954-153628955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139700954	chr7:153628996-153628997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565966651	chr7:153628997-153628998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144292678	chr7:153629029-153629030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557853617	chr7:153629081-153629082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576988918	chr7:153629092-153629093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368823819	chr7:153629121-153629122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576680609	chr7:153629181-153629182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153627200-153627400	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr7:153627400-153628200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:153627600-153628000	Enhancers	Colon Smooth Muscle	Colon
4	chr7:153627600-153629000	Enhancers	Brain Germinal Matrix	brain
5	chr7:153627800-153628200	Enhancers	Stomach Smooth Muscle	stomach
6	chr7:153628200-153628800	Enhancers	Brain Hippocampus Middle	brain
7	chr7:153628200-153629000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:153628200-153640600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr7:153628600-153629600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr7:153628800-153629200	Enhancers	Fetal Kidney	kidney
11	chr7:153628800-153629600	Weak transcription	Brain Hippocampus Middle	brain
12	chr7:153629000-153631600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:153629200-153632400	Weak transcription	Fetal Kidney	kidney
14	chr7:153629600-153629800	Enhancers	Brain Hippocampus Middle	brain
15	chr7:153629600-153631200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:153629800-153630000	Weak transcription	Brain Hippocampus Middle	brain
17	chr7:153630800-153631000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr7:153630800-153632000	Enhancers	Fetal Muscle Leg	muscle
19	chr7:153630800-153632400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:153631000-153643000	Weak transcription	Right Atrium	heart
21	chr7:153631200-153631400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:153631600-153631800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr7:153631600-153632200	Enhancers	Brain Substantia Nigra	brain
24	chr7:153631600-153632800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:153631800-153632000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
26	chr7:153631800-153632000	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr7:153631800-153632000	Bivalent Enhancer	Fetal Brain Male	brain
28	chr7:153631800-153632200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:153631800-153632200	Bivalent Enhancer	Brain Angular Gyrus	brain
30	chr7:153631800-153632200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:153631800-153632200	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr7:153632000-153632200	Bivalent/Poised TSS	Fetal Stomach	stomach
33	chr7:153632000-153632400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
34	chr7:153632200-153632400	Enhancers	Fetal Brain Female	brain
35	chr7:153632200-153635800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr7:153632200-153641200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:153632400-153632600	Enhancers	Fetal Kidney	kidney
38	chr7:153632400-153632600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr7:153632600-153636400	Weak transcription	Fetal Kidney	kidney
40	chr7:153633400-153633600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr7:153635800-153636000	Enhancers	Gastric	stomach
42	chr7:153635800-153637000	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:153636000-153636600	Weak transcription	Gastric	stomach
44	chr7:153636400-153636800	Enhancers	Fetal Lung	lung
45	chr7:153636400-153637000	Enhancers	Fetal Kidney	kidney
46	chr7:153636600-153636800	Bivalent Enhancer	Fetal Brain Male	brain
47	chr7:153636600-153637800	Enhancers	Gastric	stomach
48	chr7:153637000-153638000	Bivalent Enhancer	Fetal Brain Female	brain
49	chr7:153637000-153638000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr7:153637000-153640200	Weak transcription	Fetal Kidney	kidney

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