Variant report

Variant	nsv525557
Chromosome Location	chr1:74977705-74991644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr1:74987849-74988223	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr1:74978216-74978383	K562	blood:	n/a	n/a
3	CTCF	chr1:74983224-74983368	GM12878	blood:	n/a	n/a
4	CTCF	chr1:74983144-74983405	GM12878	blood:	n/a	n/a
5	CTCF	chr1:74978260-74978410	HRPEpiC	eye:	n/a	n/a
6	CTCF	chr1:74981254-74981317	GM13977	blood:	n/a	n/a
7	CTCF	chr1:74978260-74978410	HEK293	kidney:	n/a	n/a
8	CTCF	chr1:74978240-74978390	WERI-Rb-1	eye:	n/a	n/a
9	EBF1	chr1:74983367-74983776	GM12878	blood:	n/a	chr1:74983586-74983597
10	EBF1	chr1:74983462-74983698	GM12878	blood:	n/a	chr1:74983586-74983597
11	EBF1	chr1:74983392-74983710	GM12878	blood:	n/a	chr1:74983586-74983597
12	FOS	chr1:74979313-74979435	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr1:74979310-74979487	MCF10A-Er-Src	breast:	n/a	n/a
14	FOSL2	chr1:74984463-74984622	HepG2	liver:	n/a	n/a
15	GABPA	chr1:74984504-74984588	HepG2	liver:	n/a	n/a
16	GTF2F1	chr1:74987889-74987951	H1-hESC	embryonic stem cell:	n/a	n/a
17	JUN	chr1:74978025-74978240	HepG2	liver:	n/a	chr1:74978086-74978099 chr1:74978036-74978047
18	JUND	chr1:74987839-74988269	H1-hESC	embryonic stem cell:	n/a	n/a
19	JUND	chr1:74977908-74978257	HepG2	liver:	n/a	chr1:74978036-74978047
20	MAX	chr1:74978303-74978533	H1-hESC	embryonic stem cell:	n/a	n/a
21	MYC	chr1:74979260-74979389	MCF10A-Er-Src	breast:	n/a	n/a
22	MYC	chr1:74978395-74978401	MCF10A-Er-Src	breast:	n/a	n/a
23	NANOG	chr1:74987840-74988095	H1-hESC	embryonic stem cell:	n/a	n/a
24	NANOG	chr1:74989872-74990162	H1-hESC	embryonic stem cell:	n/a	n/a
25	PBX3	chr1:74984495-74984590	GM12878	blood:	n/a	n/a
26	POLR2A	chr1:74986120-74986263	K562	blood:	n/a	n/a
27	POLR2A	chr1:74979097-74979462	H1-neurons	neurons:	n/a	n/a
28	POLR2A	chr1:74984829-74985419	K562	blood:	n/a	n/a
29	RAD21	chr1:74983192-74983394	GM12878	blood:	n/a	n/a
30	RAD21	chr1:74983196-74983353	GM12878	blood:	n/a	n/a
31	RAD21	chr1:74978134-74978474	H1-hESC	embryonic stem cell:	n/a	n/a
32	REST	chr1:74987533-74988584	H1-neurons	neurons:	n/a	n/a
33	REST	chr1:74987739-74988340	H1-neurons	neurons:	n/a	n/a
34	RFX5	chr1:74988355-74988411	K562	blood:	n/a	n/a
35	SP1	chr1:74987697-74988264	H1-hESC	embryonic stem cell:	n/a	n/a
36	SPI1	chr1:74983127-74983554	GM12891	blood:	n/a	n/a
37	SPI1	chr1:74983239-74983554	GM12891	blood:	n/a	n/a
38	SPI1	chr1:74983234-74983500	GM12878	blood:	n/a	n/a
39	STAT1	chr1:74983222-74983235	GM12878	blood:	n/a	n/a
40	TCF12	chr1:74987847-74988121	H1-hESC	embryonic stem cell:	n/a	n/a
41	TCF12	chr1:74987773-74988059	H1-hESC	embryonic stem cell:	n/a	n/a
42	TEAD4	chr1:74987819-74988303	H1-hESC	embryonic stem cell:	n/a	n/a
43	TEAD4	chr1:74987816-74988318	H1-hESC	embryonic stem cell:	n/a	n/a
44	USF2	chr1:74977820-74978009	HepG2	liver:	n/a	n/a
45	ZNF143	chr1:74978267-74978340	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74988194-74988244	NB4	blood:	n/a
2	chr1:74988194-74988244	A549	lung:	n/a
3	chr1:74988194-74988244	HCPEpiC	choroid plexus:	n/a
4	chr1:74988194-74988244	GM12892	blood:	n/a
5	chr1:74988194-74988244	Hela-S3	cervix:	n/a
6	chr1:74988194-74988244	SAEC	small airway:	n/a
7	chr1:74988194-74988244	NH-A	brain:	n/a
8	chr1:74988194-74988244	HMEC	breast:	n/a
9	chr1:74988194-74988244	U87	brain:	n/a
10	chr1:74988194-74988244	PFSK-1	brain:	n/a
11	chr1:74988194-74988244	Jurkat	blood:	n/a
12	chr1:74988194-74988244	Caco-2	colon:	n/a
13	chr1:74988194-74988244	GM12878	blood:	n/a
14	chr1:74988194-74988244	HepG2	liver:	n/a
15	chr1:74988194-74988244	RPTEC	kidney:	n/a
16	chr1:74988194-74988244	GM06990	blood:	n/a
17	chr1:74988194-74988244	HEK293	kidney:	embryo
18	chr1:74988194-74988244	HRE	kidney:	n/a
19	chr1:74988194-74988244	HEEpiC	esophagus:	n/a
20	chr1:74988194-74988244	AG04449	skin:	fetal
21	chr1:74988194-74988244	H1-hESC	embryonic stem cell:	embryo
22	chr1:74988194-74988244	BE2_C	brain:	n/a
23	chr1:74988194-74988244	IMR90	lung:	fetal
24	chr1:74988194-74988244	AG09319	gingival:	n/a
25	chr1:74988194-74988244	HRCEpiC	kidney:	n/a
26	chr1:74988194-74988244	HCM	heart:	n/a
27	chr1:74988194-74988244	MCF10A-Er-Src	breast:	n/a
28	chr1:74988194-74988244	HIPEpiC	eye:	n/a
29	chr1:74988194-74988244	GM12891	blood:	n/a
30	chr1:74988194-74988244	K562	blood:	n/a
31	chr1:74988194-74988244	SK-N-SH	brain:	n/a
32	chr1:74988194-74988244	AG10803	skin:	n/a
33	chr1:74988194-74988244	PANC-1	pancreas:	n/a
34	chr1:74988194-74988244	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:74988194-74988244	BJ	skin:	n/a
36	chr1:74988194-74988244	HNPCEpiC	eye:	n/a
37	chr1:74988194-74988244	T-47D	breast:	n/a
38	chr1:74988194-74988244	ProgFib	skin:	n/a
39	chr1:74988194-74988244	HL-60	blood:	n/a
40	chr1:74988194-74988244	GM19239	blood:	n/a
41	chr1:74988194-74988244	SK-N-MC	brain:	n/a
42	chr1:74988194-74988244	MCF-7	breast:	n/a
43	chr1:74988194-74988244	HCF	heart:	n/a
44	chr1:74988194-74988244	AG04450	lung:	fetal
45	chr1:74988194-74988244	AG09309	skin:	n/a
46	chr1:74988194-74988244	NHDF-neo	bronchial:	n/a
47	chr1:74988194-74988244	Hepatocyte	liver:	n/a
48	chr1:74988194-74988244	HRPEpiC	eye:	n/a
49	chr1:74988194-74988244	ECC-1	luminal epithelium:	n/a
50	chr1:74988194-74988244	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:74977554..74979985-chr1:75198825..75201036,2	K562	blood:
2	chr1:74990321..74992157-chr1:75009741..75011754,2	K562	blood:

No data

Variant related genes	Relation type
LRRC53	TF binding region
LRRC53	CpG island
ENSG00000162623	chromatin interactions
ENSG00000116791	chromatin interactions

Extended variants
information (count: 581 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1040071	chr1:74977705-74977706	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs185996908	chr1:74977736-74977737	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs141734637	chr1:74977742-74977743	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531383011	chr1:74977835-74977836	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs34250428	chr1:74977840-74977841	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs116745199	chr1:74977850-74977851	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1040070	chr1:74977870-74977871	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs529360455	chr1:74977873-74977874	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs150550408	chr1:74977917-74977918	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs191384463	chr1:74977929-74977930	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534222482	chr1:74977941-74977942	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs551767054	chr1:74977943-74977944	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183213928	chr1:74977944-74977945	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs72979498	chr1:74977954-74977955	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs58737338	chr1:74977974-74977975	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573896110	chr1:74977988-74977989	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369394631	chr1:74977993-74977994	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190611171	chr1:74977997-74977998	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553466551	chr1:74978067-74978068	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2175875	chr1:74978083-74978084	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550084498	chr1:74978123-74978124	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs17095489	chr1:74978128-74978129	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs79298958	chr1:74978160-74978161	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375947096	chr1:74978175-74978176	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535148497	chr1:74978217-74978218	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182343818	chr1:74978305-74978306	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs550550434	chr1:74978308-74978309	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs564216193	chr1:74978317-74978318	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs576247128	chr1:74978318-74978319	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs543355877	chr1:74978352-74978353	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs568719348	chr1:74978394-74978395	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs370348951	chr1:74978541-74978542	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537485143	chr1:74978561-74978562	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561893171	chr1:74978562-74978563	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs529119536	chr1:74978567-74978568	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547899298	chr1:74978600-74978601	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559916070	chr1:74978622-74978623	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs533364707	chr1:74978638-74978639	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144558804	chr1:74978642-74978643	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs139575201	chr1:74978654-74978655	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569957716	chr1:74978669-74978670	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537700514	chr1:74978691-74978692	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs143661090	chr1:74978709-74978710	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs567485819	chr1:74978713-74978714	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534921774	chr1:74978750-74978751	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs553427830	chr1:74978797-74978798	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs187774889	chr1:74978805-74978806	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539169480	chr1:74978834-74978835	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs553941711	chr1:74978846-74978847	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs12027708	chr1:74978851-74978852	Enhancers Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74959800-74977800	Weak transcription	Left Ventricle	heart
2	chr1:74975600-74978400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:74975600-74978800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:74977200-74979000	Genic enhancers	Fetal Heart	heart
5	chr1:74977600-74980000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr1:74977800-74978400	Enhancers	Left Ventricle	heart
7	chr1:74978400-74978800	Weak transcription	Left Ventricle	heart
8	chr1:74978400-74980200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr1:74978600-74978800	Enhancers	Right Atrium	heart
10	chr1:74978800-74979000	Enhancers	Left Ventricle	heart
11	chr1:74978800-74979600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:74978800-74989800	Weak transcription	Right Atrium	heart
13	chr1:74979000-74986400	Weak transcription	Left Ventricle	heart
14	chr1:74979000-74986800	Weak transcription	Fetal Heart	heart
15	chr1:74979600-74987800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:74980000-74987800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr1:74983000-74984400	Enhancers	GM12878-XiMat	blood
18	chr1:74983600-74987200	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr1:74986400-74986800	Enhancers	Left Ventricle	heart
20	chr1:74986600-74986800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:74986800-74988200	Enhancers	Fetal Heart	heart
22	chr1:74986800-74989200	Weak transcription	Left Ventricle	heart
23	chr1:74986800-74989600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:74987000-74987600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr1:74987200-74987800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:74987200-74987800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:74987200-74987800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr1:74987200-74989800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:74987200-74992400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:74987400-74987600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr1:74987400-74988400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:74987600-74988000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr1:74987600-74988200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr1:74987600-74988400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:74987600-74988400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr1:74987600-74988600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr1:74987800-74988000	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:74987800-74988200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr1:74987800-74988200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr1:74987800-74988200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:74987800-74988400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:74987800-74988400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr1:74987800-74988600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr1:74987800-74988600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:74987800-74988800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:74987800-74988800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:74987800-74988800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:74987800-74988800	Enhancers	HSMMtube	muscle
49	chr1:74988000-74988400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:74988000-74990400	Enhancers	H9 Cell Line	embryonic stem cell

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