Variant report

Variant	nsv1034492
Chromosome Location	chr8:99436341-99456516
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	chr8:99439051-99439621	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:99439984-99440418	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr8:99439105-99439256	GM12878	blood:	n/a	chr8:99439120-99439136 chr8:99439119-99439135
4	BHLHE40	chr8:99439044-99439255	K562	blood:	n/a	chr8:99439120-99439136 chr8:99439119-99439135
5	CCNT2	chr8:99439046-99439246	K562	blood:	n/a	n/a
6	CEBPB	chr8:99437887-99438183	A549	lung:	n/a	chr8:99438052-99438063 chr8:99438010-99438023
7	CEBPB	chr8:99452549-99452810	A549	lung:	n/a	chr8:99452648-99452659
8	CEBPB	chr8:99452522-99452799	K562	blood:	n/a	chr8:99452648-99452659
9	CEBPB	chr8:99437980-99438087	H1-hESC	embryonic stem cell:	n/a	chr8:99438052-99438063 chr8:99438010-99438023
10	CEBPB	chr8:99437959-99438019	K562	blood:	n/a	n/a
11	CEBPB	chr8:99452582-99452814	MCF-7	breast:	n/a	chr8:99452648-99452659
12	CEBPB	chr8:99452597-99452684	H1-hESC	embryonic stem cell:	n/a	chr8:99452648-99452659
13	CEBPB	chr8:99437879-99438185	HepG2	liver:	n/a	chr8:99438052-99438063 chr8:99438010-99438023
14	CEBPB	chr8:99452509-99452800	HepG2	liver:	n/a	chr8:99452648-99452659
15	CEBPB	chr8:99452516-99452812	IMR90	lung:	n/a	chr8:99452648-99452659
16	CHD2	chr8:99440099-99440424	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr8:99438884-99439356	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:99440080-99440230	RPTEC	kidney:	n/a	chr8:99440117-99440130
19	CTCF	chr8:99455754-99455760	LNCaP	prostate:	n/a	n/a
20	CTCF	chr8:99440160-99440310	HMF	breast:	n/a	n/a
21	CTCF	chr8:99440140-99440290	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr8:99440086-99440280	NHEK	skin:	n/a	chr8:99440117-99440130
23	CTCF	chr8:99440099-99440273	A549	lung:	n/a	chr8:99440117-99440130
24	CTCF	chr8:99440080-99440230	AG09319	gingival:	n/a	chr8:99440117-99440130
25	CTCF	chr8:99439963-99440415	H1-hESC	embryonic stem cell:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
26	CTCF	chr8:99440120-99440270	HEK293	kidney:	n/a	n/a
27	CTCF	chr8:99440000-99440150	HMEC	breast:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
28	CTCF	chr8:99440100-99440250	HFF	foreskin:	n/a	chr8:99440117-99440130
29	CTCF	chr8:99443700-99443850	GM12864	blood:	n/a	n/a
30	CTCF	chr8:99439880-99440030	SAEC	small airway:	n/a	n/a
31	CTCF	chr8:99440120-99440270	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr8:99440080-99440230	SAEC	small airway:	n/a	chr8:99440117-99440130
33	CTCF	chr8:99440120-99440270	GM12867	blood:	n/a	n/a
34	CTCF	chr8:99455762-99455815	LNCaP	prostate:	n/a	n/a
35	CTCF	chr8:99440160-99440310	HCM	heart:	n/a	n/a
36	CTCF	chr8:99440120-99440270	HCFaa	heart:	n/a	n/a
37	CTCF	chr8:99440020-99440170	GM12869	blood:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
38	CTCF	chr8:99440060-99440209	HepG2	liver:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
39	CTCF	chr8:99440093-99440294	IMR90	lung:	n/a	chr8:99440117-99440130
40	CTCF	chr8:99440060-99440210	GM06990	blood:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
41	CTCF	chr8:99439145-99439151	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr8:99440020-99440170	GM12874	blood:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
43	CTCF	chr8:99440140-99440290	GM12875	blood:	n/a	n/a
44	CTCF	chr8:99440100-99440250	HRPEpiC	eye:	n/a	chr8:99440117-99440130
45	CTCF	chr8:99440065-99440223	SK-N-SH_RA	brain:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
46	CTCF	chr8:99440050-99440354	H1-hESC	embryonic stem cell:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
47	CTCF	chr8:99440020-99440170	WI-38	lung:	n/a	chr8:99440117-99440130 chr8:99440070-99440079
48	CTCF	chr8:99440117-99440294	Fibrobl	skin:	n/a	chr8:99440117-99440130
49	CTCF	chr8:99440160-99440310	BJ	skin:	n/a	n/a
50	CTCF	chr8:99440080-99440230	GM12868	blood:	n/a	chr8:99440117-99440130

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99439441-99439491	HRE	kidney:	n/a
2	chr8:99438968-99439018	U87	brain:	n/a
3	chr8:99440279-99440329	HUVEC	blood vessel:	n/a
4	chr8:99440279-99440329	Jurkat	blood:	n/a
5	chr8:99438624-99438674	NH-A	brain:	n/a
6	chr8:99438624-99438674	ProgFib	skin:	n/a
7	chr8:99439119-99439169	BJ	skin:	n/a
8	chr8:99442883-99442933	HEK293	kidney:	embryo
9	chr8:99439948-99439998	HCT-116	colon:	n/a
10	chr8:99440279-99440329	AG09319	gingival:	n/a
11	chr8:99442883-99442933	GM19239	blood:	n/a
12	chr8:99439861-99439911	AG10803	skin:	n/a
13	chr8:99440331-99440381	HEK293	kidney:	embryo
14	chr8:99439119-99439169	Hela-S3	cervix:	n/a
15	chr8:99440279-99440329	A549	lung:	n/a
16	chr8:99439685-99439735	GM19239	blood:	n/a
17	chr8:99439861-99439911	HRE	kidney:	n/a
18	chr8:99438624-99438674	HRE	kidney:	n/a
19	chr8:99439861-99439911	RPTEC	kidney:	n/a
20	chr8:99438968-99439018	HRE	kidney:	n/a
21	chr8:99439119-99439169	SK-N-SH_RA	brain:	n/a
22	chr8:99439948-99439998	HMEC	breast:	n/a
23	chr8:99439948-99439998	MCF-7	breast:	n/a
24	chr8:99440522-99440572	HCT-116	colon:	n/a
25	chr8:99439948-99439998	SKMC	muscle:	n/a
26	chr8:99439119-99439169	ECC-1	luminal epithelium:	n/a
27	chr8:99438968-99439018	PrEC	prostate:	n/a
28	chr8:99439948-99439998	T-47D	breast:	n/a
29	chr8:99439119-99439169	HUVEC	blood vessel:	n/a
30	chr8:99439119-99439169	H1-hESC	embryonic stem cell:	embryo
31	chr8:99442883-99442933	GM12878	blood:	n/a
32	chr8:99442883-99442933	SKMC	muscle:	n/a
33	chr8:99439861-99439911	PANC-1	pancreas:	n/a
34	chr8:99442883-99442933	AG04449	skin:	fetal
35	chr8:99440331-99440381	H1-hESC	embryonic stem cell:	embryo
36	chr8:99440279-99440329	CMK	blood:	n/a
37	chr8:99441950-99442000	HAEpiC	amniotic membrane:	n/a
38	chr8:99438624-99438674	HUVEC	blood vessel:	n/a
39	chr8:99439685-99439735	GM12878	blood:	n/a
40	chr8:99438942-99438992	GM12891	blood:	n/a
41	chr8:99440279-99440329	ECC-1	luminal epithelium:	n/a
42	chr8:99439119-99439169	Caco-2	colon:	n/a
43	chr8:99439861-99439911	AG04449	skin:	fetal
44	chr8:99439685-99439735	AoSMC	blood vessel:	n/a
45	chr8:99439948-99439998	LNCaP	prostate:	n/a
46	chr8:99439441-99439491	HCF	heart:	n/a
47	chr8:99438968-99439018	ovcar-3	ovarian:	n/a
48	chr8:99441950-99442000	IMR90	lung:	fetal
49	chr8:99438942-99438992	AG10803	skin:	n/a
50	chr8:99439861-99439911	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:99444054..99446996-chr8:99450505..99452269,2	MCF-7	breast:
2	chr8:99413566..99415958-chr8:99440640..99443091,2	MCF-7	breast:
3	chr8:99444965..99447150-chr8:99453848..99455622,2	MCF-7	breast:
4	chr12:27340912..27341732-chr8:99449571..99450562,2	MCF-7	breast:
5	chr8:99444965..99447150-chr8:99453848..99455622,2	MCF-7	breast:
6	chr8:99448661..99451637-chr8:99454242..99456567,3	MCF-7	breast:
7	chr8:99432751..99435716-chr8:99435816..99437707,2	MCF-7	breast:
8	chr8:99444054..99446996-chr8:99450505..99452269,2	MCF-7	breast:
9	chr8:99451152..99453654-chr8:99459310..99462023,3	MCF-7	breast:
10	chr8:99440204..99443025-chr8:99468431..99469990,2	K562	blood:
11	chr8:99455496..99458088-chr8:99462894..99465787,2	MCF-7	breast:
12	chr8:99433334..99435715-chr8:99442635..99445269,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNS2-2	chr8:99448897-99451518	ENSG00000272321.1

Variant related genes	Relation type
KCNS2	TF binding region
ENSG00000272321	TF binding region
KCNS2	CpG island
ENSG00000272321	CpG island
ENSG00000272321	chromatin interactions

Extended variants
information (count: 693 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7826857	chr8:99436341-99436342	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10808360	chr8:99436354-99436355	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs10955173	chr8:99436357-99436358	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs186185468	chr8:99436376-99436377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528838329	chr8:99436382-99436383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549336113	chr8:99436398-99436399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562766321	chr8:99436457-99436458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531562670	chr8:99436505-99436506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34039625	chr8:99436528-99436529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140768320	chr8:99436566-99436567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571384872	chr8:99436572-99436573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527787138	chr8:99436576-99436577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539570922	chr8:99436645-99436646	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150095005	chr8:99436646-99436647	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374252334	chr8:99436672-99436673	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535449635	chr8:99436710-99436711	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560966189	chr8:99436767-99436768	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190908164	chr8:99436792-99436793	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575512588	chr8:99436835-99436836	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538086380	chr8:99436920-99436921	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183325665	chr8:99436926-99436927	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578104474	chr8:99437011-99437012	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4236852	chr8:99437024-99437025	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs550135696	chr8:99437026-99437027	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560181978	chr8:99437043-99437044	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573723782	chr8:99437078-99437079	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542620819	chr8:99437101-99437102	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116197596	chr8:99437108-99437109	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145444566	chr8:99437125-99437126	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4076778	chr8:99437142-99437143	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564935026	chr8:99437160-99437161	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61084869	chr8:99437166-99437167	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79374531	chr8:99437200-99437201	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546820444	chr8:99437208-99437209	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566954756	chr8:99437258-99437259	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529278114	chr8:99437290-99437291	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs187590215	chr8:99437350-99437351	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs568880673	chr8:99437387-99437388	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs112237105	chr8:99437427-99437428	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs558385238	chr8:99437446-99437447	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs111262114	chr8:99437447-99437448	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs571785482	chr8:99437465-99437466	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs190774501	chr8:99437523-99437524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs73273953	chr8:99437538-99437539	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183014800	chr8:99437542-99437543	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs570936450	chr8:99437556-99437557	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs72444718	chr8:99437557-99437558	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs149252515	chr8:99437567-99437568	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs72287836	chr8:99437568-99437569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs116916066	chr8:99437570-99437571	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99428400-99438200	Weak transcription	Pancreas	Pancrea
2	chr8:99429000-99437000	Weak transcription	Spleen	Spleen
3	chr8:99430400-99437400	Enhancers	Fetal Heart	heart
4	chr8:99436600-99436800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr8:99436600-99436800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:99436600-99436800	Bivalent Enhancer	Fetal Thymus	thymus
7	chr8:99436600-99437200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:99436600-99437200	Enhancers	Brain Angular Gyrus	brain
9	chr8:99437200-99437400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:99437400-99437800	Weak transcription	Fetal Heart	heart
11	chr8:99437800-99438200	Enhancers	Fetal Heart	heart
12	chr8:99437800-99438400	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr8:99437800-99438600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:99438000-99439200	Bivalent/Poised TSS	Brain Angular Gyrus	brain
15	chr8:99438000-99440200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:99438000-99440600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr8:99438000-99440600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr8:99438000-99441200	ZNF genes & repeats	Spleen	Spleen
19	chr8:99438200-99438400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:99438200-99438400	Bivalent/Poised TSS	Adipose Nuclei	Adipose
21	chr8:99438200-99438400	Enhancers	Ovary	ovary
22	chr8:99438200-99438400	Enhancers	Pancreas	Pancrea
23	chr8:99438200-99438600	Bivalent Enhancer	Fetal Heart	heart
24	chr8:99438200-99438600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
25	chr8:99438200-99438800	Bivalent Enhancer	Fetal Stomach	stomach
26	chr8:99438200-99440200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:99438400-99438600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
28	chr8:99438400-99438600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:99438400-99438600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:99438400-99438600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:99438400-99438600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr8:99438400-99438600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr8:99438400-99438600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
34	chr8:99438400-99438600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
35	chr8:99438400-99438600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr8:99438400-99438600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
37	chr8:99438400-99438600	Bivalent/Poised TSS	Fetal Brain Male	brain
38	chr8:99438400-99438600	Flanking Bivalent TSS/Enh	NHDF-Ad	bronchial
39	chr8:99438400-99438800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
40	chr8:99438400-99438800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chr8:99438400-99438800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:99438400-99438800	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr8:99438400-99438800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr8:99438400-99438800	Bivalent Enhancer	Colon Smooth Muscle	Colon
45	chr8:99438400-99438800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr8:99438400-99438800	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr8:99438400-99438800	Flanking Active TSS	Ovary	ovary
48	chr8:99438400-99438800	Bivalent/Poised TSS	Right Ventricle	heart
49	chr8:99438400-99438800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr8:99438400-99439000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain

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