Variant report

Variant	nsv546757
Chromosome Location	chr1:86412177-86509996
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	ATF2	chr1:86481849-86482390	GM12878	blood:	n/a	n/a
2	ATF2	chr1:86458295-86458893	GM12878	blood:	n/a	n/a
3	ATF2	chr1:86480984-86481436	GM12878	blood:	n/a	n/a
4	ATF2	chr1:86480950-86481529	GM12878	blood:	n/a	n/a
5	ATF2	chr1:86481680-86482390	GM12878	blood:	n/a	n/a
6	BACH1	chr1:86466630-86466716	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:86458496-86458770	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:86481037-86481412	GM12878	blood:	n/a	chr1:86481190-86481201
9	BATF	chr1:86482063-86482352	GM12878	blood:	n/a	chr1:86482241-86482249
10	BATF	chr1:86481061-86481297	GM12878	blood:	n/a	chr1:86481190-86481201
11	BATF	chr1:86481768-86482372	GM12878	blood:	n/a	chr1:86482241-86482249
12	BCL11A	chr1:86481010-86481417	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:86481786-86482316	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:86484035-86484272	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr1:86480994-86481161	IMR90	lung:	n/a	chr1:86481078-86481091
16	CEBPB	chr1:86462839-86463118	IMR90	lung:	n/a	chr1:86462982-86462993 chr1:86462983-86462994
17	CEBPB	chr1:86476191-86476298	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:86462839-86463120	HepG2	liver:	n/a	chr1:86462982-86462993 chr1:86462983-86462994
19	CEBPB	chr1:86465462-86465662	HepG2	liver:	n/a	chr1:86465553-86465564
20	CEBPB	chr1:86497465-86497549	K562	blood:	n/a	chr1:86497510-86497519 chr1:86497510-86497519 chr1:86497510-86497519 chr1:86497508-86497521 chr1:86497510-86497519 chr1:86497510-86497521
21	CEBPB	chr1:86462907-86463108	A549	lung:	n/a	chr1:86462982-86462993 chr1:86462983-86462994
22	CEBPB	chr1:86463892-86464199	IMR90	lung:	n/a	n/a
23	CHD1	chr1:86442140-86442259	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:86427410-86427663	HepG2	liver:	n/a	n/a
25	CREB1	chr1:86458468-86458909	GM12878	blood:	n/a	n/a
26	CTCF	chr1:86484100-86484250	HMEC	breast:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
27	CTCF	chr1:86465003-86465089	GM12891	blood:	n/a	n/a
28	CTCF	chr1:86484080-86484230	HBMEC	blood vessel:	n/a	chr1:86484174-86484182 chr1:86484164-86484185 chr1:86484170-86484186 chr1:86484169-86484187
29	CTCF	chr1:86484091-86484277	MCF-7	breast:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
30	CTCF	chr1:86484104-86484307	GM20000	blood:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
31	CTCF	chr1:86484080-86484230	AG09319	gingival:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
32	CTCF	chr1:86474067-86474092	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:86483220-86483370	AG10803	skin:	n/a	n/a
34	CTCF	chr1:86484064-86484289	Pancreas_OC	pancreas:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
35	CTCF	chr1:86484120-86484270	NHEK	skin:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
36	CTCF	chr1:86484020-86484170	HFF	foreskin:	n/a	n/a
37	CTCF	chr1:86484100-86484250	HUVEC	blood vessel:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
38	CTCF	chr1:86484120-86484270	AoAF	blood vessel:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
39	CTCF	chr1:86484066-86484212	SK-N-SH_RA	brain:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
40	CTCF	chr1:86484100-86484250	HEEpiC	esophagus:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
41	CTCF	chr1:86483816-86484564	A549	lung:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
42	CTCF	chr1:86484100-86484250	HEK293	kidney:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
43	CTCF	chr1:86485814-86485874	GM20000	blood:	n/a	n/a
44	CTCF	chr1:86484100-86484250	GM12867	blood:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
45	CTCF	chr1:86484100-86484250	HPF	lung:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
46	CTCF	chr1:86420820-86420970	HEK293	kidney:	n/a	n/a
47	CTCF	chr1:86484066-86484305	GM13977	blood:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
48	CTCF	chr1:86484080-86484230	HAc	cerebellar:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
49	CTCF	chr1:86484120-86484270	HA-sp	spinal cord:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185
50	CTCF	chr1:86484060-86484210	GM12868	blood:	n/a	chr1:86484174-86484182 chr1:86484170-86484186 chr1:86484169-86484187 chr1:86484164-86484185

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86429211-86429261	HCM	heart:	n/a
2	chr1:86429211-86429261	K562	blood:	n/a
3	chr1:86429211-86429261	IMR90	lung:	fetal
4	chr1:86429211-86429261	AG09309	skin:	n/a
5	chr1:86429211-86429261	HL-60	blood:	n/a
6	chr1:86429211-86429261	HIPEpiC	eye:	n/a
7	chr1:86429211-86429261	Hela-S3	cervix:	n/a
8	chr1:86429211-86429261	NH-A	brain:	n/a
9	chr1:86429211-86429261	HUVEC	blood vessel:	n/a
10	chr1:86429211-86429261	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:86429211-86429261	Jurkat	blood:	n/a
12	chr1:86429211-86429261	SK-N-SH_RA	brain:	n/a
13	chr1:86429211-86429261	SK-N-SH	brain:	n/a
14	chr1:86429211-86429261	NHDF-neo	bronchial:	n/a
15	chr1:86429211-86429261	HMEC	breast:	n/a
16	chr1:86429211-86429261	BE2_C	brain:	n/a
17	chr1:86429211-86429261	U87	brain:	n/a
18	chr1:86429211-86429261	SKMC	muscle:	n/a
19	chr1:86429211-86429261	SAEC	small airway:	n/a
20	chr1:86429211-86429261	NB4	blood:	n/a
21	chr1:86429211-86429261	ECC-1	luminal epithelium:	n/a
22	chr1:86429211-86429261	HepG2	liver:	n/a
23	chr1:86429211-86429261	PrEC	prostate:	n/a
24	chr1:86429211-86429261	NT2-D1	testis:	n/a
25	chr1:86429211-86429261	BJ	skin:	n/a
26	chr1:86429211-86429261	GM12878	blood:	n/a
27	chr1:86429211-86429261	ovcar-3	ovarian:	n/a
28	chr1:86429211-86429261	ProgFib	skin:	n/a
29	chr1:86429211-86429261	GM06990	blood:	n/a
30	chr1:86429211-86429261	GM19239	blood:	n/a
31	chr1:86429211-86429261	HEK293	kidney:	embryo
32	chr1:86429211-86429261	RPTEC	kidney:	n/a
33	chr1:86429211-86429261	AG10803	skin:	n/a
34	chr1:86429211-86429261	HCT-116	colon:	n/a
35	chr1:86429211-86429261	GM12891	blood:	n/a
36	chr1:86429211-86429261	HCF	heart:	n/a
37	chr1:86429211-86429261	GM12892	blood:	n/a
38	chr1:86429211-86429261	AG09319	gingival:	n/a
39	chr1:86429211-86429261	HCPEpiC	choroid plexus:	n/a
40	chr1:86429211-86429261	HRE	kidney:	n/a
41	chr1:86429211-86429261	T-47D	breast:	n/a
42	chr1:86429211-86429261	LNCaP	prostate:	n/a
43	chr1:86429211-86429261	AoSMC	blood vessel:	n/a
44	chr1:86429211-86429261	A549	lung:	n/a
45	chr1:86429211-86429261	CMK	blood:	n/a
46	chr1:86429211-86429261	MCF-7	breast:	n/a
47	chr1:86429211-86429261	HAEpiC	amniotic membrane:	n/a
48	chr1:86429211-86429261	Caco-2	colon:	n/a
49	chr1:86429211-86429261	AG04450	lung:	fetal
50	chr1:86429211-86429261	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:86483581..86486265-chr1:86488492..86490836,2	K562	blood:
2	chr1:86452263..86454852-chr1:86455069..86456770,2	MCF-7	breast:
3	chr1:86478740..86480612-chr1:86522997..86525923,2	K562	blood:
4	chr1:86452263..86454852-chr1:86455069..86456770,2	MCF-7	breast:
5	chr1:86360081..86361020-chr1:86483694..86484478,3	MCF-7	breast:
6	chr1:86048046..86050238-chr1:86420456..86423004,2	K562	blood:
7	chr1:86483581..86486265-chr1:86488492..86490836,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLCA2-1	chr1:86495537-86496272	NONHSAT004263

Variant related genes	Relation type
ENSG00000229505	TF binding region
ENSG00000229505	CpG island

Extended variants
information (count: 3709 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3709 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11161711	chr1:86412177-86412178	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190108739	chr1:86412192-86412193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559945644	chr1:86412223-86412224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546201484	chr1:86412287-86412288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567307895	chr1:86412299-86412300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536375379	chr1:86412332-86412333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78707552	chr1:86412491-86412492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181497122	chr1:86412502-86412503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184138355	chr1:86412539-86412540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188541389	chr1:86412540-86412541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575519593	chr1:86412544-86412545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544142378	chr1:86412556-86412557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554582897	chr1:86412571-86412572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574461074	chr1:86412577-86412578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180840846	chr1:86412638-86412639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560280126	chr1:86412639-86412640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185785251	chr1:86412644-86412645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545585513	chr1:86412676-86412677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570980293	chr1:86412689-86412690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12567297	chr1:86412690-86412691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115131577	chr1:86412702-86412703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192347188	chr1:86412734-86412735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138465894	chr1:86412737-86412738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530028388	chr1:86412751-86412752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546551837	chr1:86412818-86412819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181978730	chr1:86412856-86412857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12567480	chr1:86412857-86412858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187279475	chr1:86412868-86412869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143923076	chr1:86412898-86412899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568940841	chr1:86412908-86412909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190770997	chr1:86412955-86412956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554898190	chr1:86412977-86412978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574525807	chr1:86412978-86412979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540241973	chr1:86413018-86413019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12723176	chr1:86413022-86413023	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs147264963	chr1:86413040-86413041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138724387	chr1:86413069-86413070	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531038496	chr1:86413081-86413082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72712765	chr1:86413112-86413113	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149340358	chr1:86413119-86413120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533392795	chr1:86413120-86413121	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558661211	chr1:86413149-86413150	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17128505	chr1:86413212-86413213	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530285604	chr1:86413238-86413239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71582965	chr1:86413252-86413253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74097620	chr1:86413262-86413263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs566005137	chr1:86413278-86413279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183000832	chr1:86413280-86413281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs201394742	chr1:86413330-86413331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17128506	chr1:86413359-86413360	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86404200-86416000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:86407200-86417000	Weak transcription	Fetal Lung	lung
3	chr1:86411200-86412400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:86411200-86413200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:86412000-86415600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:86412000-86420400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:86412400-86416000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:86413000-86414200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:86413200-86413600	Weak transcription	GM12878-XiMat	blood
10	chr1:86413200-86415600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr1:86413600-86413800	Enhancers	GM12878-XiMat	blood
12	chr1:86413800-86418600	Weak transcription	GM12878-XiMat	blood
13	chr1:86414200-86414600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:86414600-86415200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:86415200-86418200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:86415600-86417400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:86415600-86417400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:86416000-86417200	Strong transcription	Primary hematopoietic stem cells	blood
19	chr1:86416000-86417200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:86417000-86420400	Enhancers	Fetal Lung	lung
21	chr1:86417200-86422000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr1:86417200-86422200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr1:86417400-86420800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:86417400-86421200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr1:86418000-86418400	Enhancers	Liver	Liver
26	chr1:86418200-86418600	Enhancers	Small Intestine	intestine
27	chr1:86418200-86419000	Enhancers	Fetal Stomach	stomach
28	chr1:86418200-86419400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:86418600-86419200	Enhancers	GM12878-XiMat	blood
30	chr1:86419200-86431600	Weak transcription	GM12878-XiMat	blood
31	chr1:86419400-86420400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:86420400-86421000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr1:86420400-86421400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:86420800-86421800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:86421000-86421400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:86421200-86423800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:86421400-86441400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:86421800-86429000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:86422000-86422800	Strong transcription	Primary hematopoietic stem cells	blood
40	chr1:86422200-86424000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr1:86422800-86442400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr1:86423800-86427000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr1:86424000-86427200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:86424800-86426000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:86425200-86425800	Enhancers	Fetal Lung	lung
46	chr1:86425800-86441200	Weak transcription	Fetal Lung	lung
47	chr1:86426000-86432000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:86427000-86427600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr1:86427200-86427600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr1:86427400-86428000	Enhancers	Fetal Intestine Small	intestine

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