Variant report

Variant	nsv582513
Chromosome Location	chr2:98829237-98869914
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	ATF1	chr2:98853451-98853677	K562	blood:	n/a	n/a
2	ATF3	chr2:98853501-98853746	K562	blood:	n/a	n/a
3	ATF3	chr2:98853467-98853716	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr2:98835641-98835980	A549	lung:	n/a	chr2:98835805-98835816
5	CEBPB	chr2:98853415-98853780	Hela-S3	cervix:	n/a	chr2:98853589-98853600
6	CEBPB	chr2:98835670-98835911	Hela-S3	cervix:	n/a	chr2:98835805-98835816
7	CEBPB	chr2:98835635-98835989	IMR90	lung:	n/a	chr2:98835805-98835816
8	CEBPB	chr2:98853509-98853849	MCF-7	breast:	n/a	chr2:98853589-98853600
9	CEBPB	chr2:98836740-98836929	A549	lung:	n/a	chr2:98836832-98836841 chr2:98836832-98836841 chr2:98836832-98836841 chr2:98836830-98836841 chr2:98836830-98836843 chr2:98836832-98836841 chr2:98836830-98836843 chr2:98836832-98836843
10	CEBPB	chr2:98853411-98853776	IMR90	lung:	n/a	chr2:98853589-98853600
11	CEBPB	chr2:98853490-98853680	K562	blood:	n/a	chr2:98853589-98853600
12	CEBPB	chr2:98835631-98835991	H1-hESC	embryonic stem cell:	n/a	chr2:98835805-98835816
13	CEBPB	chr2:98853489-98853839	A549	lung:	n/a	chr2:98853589-98853600
14	CEBPB	chr2:98853529-98853715	HepG2	liver:	n/a	chr2:98853589-98853600
15	CEBPB	chr2:98835626-98835994	HepG2	liver:	n/a	chr2:98835805-98835816
16	CEBPB	chr2:98853407-98853785	HepG2	liver:	n/a	chr2:98853589-98853600
17	CEBPB	chr2:98853412-98853776	A549	lung:	n/a	chr2:98853589-98853600
18	CEBPB	chr2:98853506-98853772	K562	blood:	n/a	chr2:98853589-98853600
19	CEBPB	chr2:98836781-98836871	K562	blood:	n/a	chr2:98836832-98836841 chr2:98836832-98836841 chr2:98836832-98836841 chr2:98836830-98836841 chr2:98836830-98836843 chr2:98836832-98836841 chr2:98836830-98836843 chr2:98836832-98836843
20	CEBPB	chr2:98835625-98835972	K562	blood:	n/a	chr2:98835805-98835816
21	CEBPB	chr2:98831267-98831329	A549	lung:	n/a	n/a
22	CEBPB	chr2:98853402-98853792	K562	blood:	n/a	chr2:98853589-98853600
23	CEBPB	chr2:98836692-98836908	HepG2	liver:	n/a	chr2:98836832-98836841 chr2:98836832-98836841 chr2:98836832-98836841 chr2:98836830-98836841 chr2:98836830-98836843 chr2:98836832-98836841 chr2:98836830-98836843 chr2:98836832-98836843
24	CEBPB	chr2:98853414-98853779	H1-hESC	embryonic stem cell:	n/a	chr2:98853589-98853600
25	CEBPB	chr2:98853506-98853735	MCF-7	breast:	n/a	chr2:98853589-98853600
26	CTCF	chr2:98849280-98849430	MCF-7	breast:	n/a	n/a
27	CTCF	chr2:98851420-98851512	LNCaP	prostate:	n/a	n/a
28	CTCF	chr2:98853105-98853178	K562	blood:	n/a	n/a
29	CTCF	chr2:98851380-98851530	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr2:98851480-98851630	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr2:98853077-98853186	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr2:98853093-98853155	A549	lung:	n/a	n/a
33	CTCF	chr2:98849200-98849350	AG09319	gingival:	n/a	n/a
34	CTCF	chr2:98868286-98868306	GM13976	blood:	n/a	n/a
35	CTCF	chr2:98853101-98853147	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:98851465-98851471	GM12878	blood:	n/a	n/a
37	CTCF	chr2:98838420-98838570	HepG2	liver:	n/a	n/a
38	CTCF	chr2:98846960-98847010	ProgFib	skin:	n/a	n/a
39	CTCF	chr2:98849200-98849350	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:98851380-98851530	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr2:98849280-98849430	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr2:98849300-98849450	GM12873	blood:	n/a	n/a
43	CTCF	chr2:98838263-98838267	Fibrobl	skin:	n/a	n/a
44	CTCF	chr2:98851484-98851528	GM10266	blood:	n/a	n/a
45	CTCF	chr2:98849340-98849490	HepG2	liver:	n/a	n/a
46	E2F6	chr2:98845637-98845947	H1-hESC	embryonic stem cell:	n/a	n/a
47	E2F6	chr2:98845725-98845943	H1-hESC	embryonic stem cell:	n/a	n/a
48	EBF1	chr2:98851674-98851864	GM12878	blood:	n/a	chr2:98851774-98851787 chr2:98851776-98851785
49	EBF1	chr2:98869094-98869234	GM12878	blood:	n/a	n/a
50	ELK1	chr2:98855051-98855069	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:98865917-98865967	PANC-1	pancreas:	n/a
2	chr2:98858136-98858186	GM19239	blood:	n/a
3	chr2:98865917-98865967	HAEpiC	amniotic membrane:	n/a
4	chr2:98852895-98852945	HepG2	liver:	n/a
5	chr2:98852910-98852960	AG04450	lung:	fetal
6	chr2:98858136-98858186	GM12878	blood:	n/a
7	chr2:98852704-98852754	HIPEpiC	eye:	n/a
8	chr2:98858011-98858061	CMK	blood:	n/a
9	chr2:98858136-98858186	NHBE	bronchial:	n/a
10	chr2:98858571-98858621	Hela-S3	cervix:	n/a
11	chr2:98852910-98852960	ProgFib	skin:	n/a
12	chr2:98858136-98858186	HAEpiC	amniotic membrane:	n/a
13	chr2:98858136-98858186	MCF-7	breast:	n/a
14	chr2:98852910-98852960	GM19239	blood:	n/a
15	chr2:98858595-98858645	SK-N-MC	brain:	n/a
16	chr2:98852704-98852754	A549	lung:	n/a
17	chr2:98865917-98865967	NHDF-neo	bronchial:	n/a
18	chr2:98858595-98858645	BJ	skin:	n/a
19	chr2:98858011-98858061	ECC-1	luminal epithelium:	n/a
20	chr2:98858595-98858645	H1-hESC	embryonic stem cell:	embryo
21	chr2:98852895-98852945	GM19239	blood:	n/a
22	chr2:98858011-98858061	BE2_C	brain:	n/a
23	chr2:98852938-98852988	HRE	kidney:	n/a
24	chr2:98858595-98858645	ProgFib	skin:	n/a
25	chr2:98858011-98858061	SK-N-SH_RA	brain:	n/a
26	chr2:98852895-98852945	RPTEC	kidney:	n/a
27	chr2:98858136-98858186	ovcar-3	ovarian:	n/a
28	chr2:98858136-98858186	Caco-2	colon:	n/a
29	chr2:98866217-98866267	RPTEC	kidney:	n/a
30	chr2:98852781-98852831	IMR90	lung:	fetal
31	chr2:98866217-98866267	H1-hESC	embryonic stem cell:	embryo
32	chr2:98852781-98852831	SAEC	small airway:	n/a
33	chr2:98865917-98865967	HL-60	blood:	n/a
34	chr2:98858595-98858645	AG09309	skin:	n/a
35	chr2:98858595-98858645	PFSK-1	brain:	n/a
36	chr2:98866217-98866267	HCT-116	colon:	n/a
37	chr2:98865917-98865967	AG09319	gingival:	n/a
38	chr2:98858595-98858645	SK-N-SH	brain:	n/a
39	chr2:98852781-98852831	HepG2	liver:	n/a
40	chr2:98852704-98852754	T-47D	breast:	n/a
41	chr2:98858011-98858061	HL-60	blood:	n/a
42	chr2:98852938-98852988	AoSMC	blood vessel:	n/a
43	chr2:98852781-98852831	GM19239	blood:	n/a
44	chr2:98858595-98858645	Hela-S3	cervix:	n/a
45	chr2:98858571-98858621	HMEC	breast:	n/a
46	chr2:98858571-98858621	AG04449	skin:	fetal
47	chr2:98852910-98852960	K562	blood:	n/a
48	chr2:98858571-98858621	IMR90	lung:	fetal
49	chr2:98858571-98858621	HL-60	blood:	n/a
50	chr2:98852910-98852960	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:98838369..98840127-chr2:98845852..98848388,2	MCF-7	breast:
2	chr2:98850498..98851020-chr2:98995603..98996163,2	MCF-7	breast:
3	chr2:98704397..98705262-chr2:98850185..98851043,2	MCF-7	breast:
4	chr2:98868004..98870745-chr2:98873730..98876518,2	K562	blood:
5	chr2:98703318..98704045-chr2:98850289..98851071,3	MCF-7	breast:
6	chr2:98849964..98853776-chr2:98854233..98857105,4	MCF-7	breast:
7	chr2:98831892..98834462-chr2:98838599..98840711,2	K562	blood:
8	chr2:98611658..98614514-chr2:98866353..98868181,2	K562	blood:
9	chr2:98831892..98834462-chr2:98838599..98840711,2	K562	blood:
10	chr2:98822445..98824064-chr2:98827178..98830158,2	K562	blood:

Variant related genes	Relation type
VWA3B	TF binding region
VWA3B	CpG island
ENSG00000231635	chromatin interactions
ENSG00000168658	chromatin interactions
ENSG00000075568	chromatin interactions

Extended variants
information (count: 1012 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2122756	chr2:98829237-98829238	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180951654	chr2:98829274-98829275	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112101211	chr2:98829292-98829293	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111544421	chr2:98829293-98829294	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35422850	chr2:98829294-98829295	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs111378437	chr2:98829296-98829297	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550867889	chr2:98829380-98829381	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs561295306	chr2:98829414-98829415	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs17427272	chr2:98829441-98829442	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs150862276	chr2:98829457-98829458	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575056148	chr2:98829489-98829490	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374807061	chr2:98829494-98829495	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139233090	chr2:98829508-98829509	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115412052	chr2:98829528-98829529	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552253114	chr2:98829532-98829533	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543550599	chr2:98829545-98829546	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs76699207	chr2:98829573-98829574	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149984622	chr2:98829584-98829585	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557283991	chr2:98829648-98829649	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546046727	chr2:98829675-98829676	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574018544	chr2:98829683-98829684	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573978465	chr2:98829702-98829703	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147736098	chr2:98829742-98829743	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559451897	chr2:98829761-98829762	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114516902	chr2:98829764-98829765	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554534176	chr2:98829775-98829776	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs142622217	chr2:98829787-98829788	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543842603	chr2:98829833-98829834	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs4564827	chr2:98829846-98829847	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs530353065	chr2:98829854-98829855	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147929237	chr2:98829890-98829891	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs207462092	chr2:98829900-98829901	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112817945	chr2:98829930-98829931	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79236680	chr2:98829953-98829954	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552642570	chr2:98830005-98830006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569420927	chr2:98830014-98830015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540158150	chr2:98830022-98830023	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531127215	chr2:98830056-98830057	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs72948974	chr2:98830092-98830093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs548630186	chr2:98830131-98830132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10199463	chr2:98830162-98830163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536565042	chr2:98830220-98830221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552853915	chr2:98830244-98830245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566664234	chr2:98830284-98830285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538507471	chr2:98830314-98830315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576636223	chr2:98830325-98830326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548172292	chr2:98830352-98830353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575027700	chr2:98830373-98830374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143056538	chr2:98830382-98830383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543990715	chr2:98830410-98830411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:139 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98827600-98829800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:98827600-98830200	Enhancers	Fetal Stomach	stomach
3	chr2:98828000-98829800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:98828000-98830000	Enhancers	Colon Smooth Muscle	Colon
5	chr2:98828400-98829400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:98828400-98829600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:98828400-98829600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:98828400-98829800	Enhancers	Fetal Brain Male	brain
9	chr2:98828400-98830000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:98828600-98829400	Enhancers	Fetal Brain Female	brain
11	chr2:98828600-98829800	Enhancers	Brain Germinal Matrix	brain
12	chr2:98828800-98829600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:98828800-98829600	Enhancers	Fetal Kidney	kidney
14	chr2:98829000-98829400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr2:98829000-98829400	Weak transcription	Rectal Smooth Muscle	rectum
16	chr2:98829000-98835000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:98829200-98829600	Flanking Active TSS	Stomach Smooth Muscle	stomach
18	chr2:98829400-98830000	Enhancers	Esophagus	oesophagus
19	chr2:98829400-98830000	Enhancers	Rectal Smooth Muscle	rectum
20	chr2:98829400-98830200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:98829600-98829800	Active TSS	Stomach Smooth Muscle	stomach
22	chr2:98829800-98830000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:98829800-98830000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:98829800-98830000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:98829800-98830000	Bivalent Enhancer	Fetal Intestine Small	intestine
26	chr2:98829800-98830000	Enhancers	Gastric	stomach
27	chr2:98829800-98830000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
28	chr2:98829800-98830000	Flanking Active TSS	Stomach Smooth Muscle	stomach
29	chr2:98830000-98832800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr2:98832800-98833200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:98832800-98833400	Enhancers	NHEK	skin
32	chr2:98832800-98833600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:98832800-98833800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:98833000-98833200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr2:98833000-98833200	Enhancers	Gastric	stomach
36	chr2:98833000-98834000	Enhancers	HMEC	breast
37	chr2:98833200-98833600	Weak transcription	Gastric	stomach
38	chr2:98833600-98833800	ZNF genes & repeats	Gastric	stomach
39	chr2:98835000-98836200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:98837600-98838000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr2:98837800-98838000	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:98838000-98838200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:98838000-98838400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:98849200-98850800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr2:98849800-98851200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr2:98850400-98851200	Enhancers	Liver	Liver
47	chr2:98850400-98851400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:98850600-98851000	Enhancers	Brain Substantia Nigra	brain
49	chr2:98850600-98851000	Enhancers	Right Ventricle	heart
50	chr2:98850600-98851200	Enhancers	Left Ventricle	heart

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