Variant report

Variant	nsv874466
Chromosome Location	chr2:85909026-85939207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:777)
CpG islands
(count:673)
Chromatin interactive
region (count:27)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:85932800-85932803	K562	blood:	n/a	n/a
2	ATF1	chr2:85934398-85934782	K562	blood:	n/a	n/a
3	ATF2	chr2:85931795-85932521	GM12878	blood:	n/a	n/a
4	ATF2	chr2:85934284-85934800	GM12878	blood:	n/a	n/a
5	ATF2	chr2:85931737-85932545	GM12878	blood:	n/a	n/a
6	ATF3	chr2:85929237-85929770	HCT-116	colon:	n/a	n/a
7	ATF3	chr2:85932668-85933082	K562	blood:	n/a	n/a
8	ATF3	chr2:85932552-85933206	HCT-116	colon:	n/a	n/a
9	ATF3	chr2:85932589-85933235	HCT-116	colon:	n/a	n/a
10	BACH1	chr2:85934477-85934677	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr2:85932062-85932409	GM12878	blood:	n/a	n/a
12	BATF	chr2:85932066-85932447	GM12878	blood:	n/a	n/a
13	BATF	chr2:85934445-85934705	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:85931860-85932487	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:85932056-85932489	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:85934259-85934773	GM12878	blood:	n/a	n/a
17	BCLAF1	chr2:85932045-85932549	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:85914457-85914661	K562	blood:	n/a	chr2:85914497-85914506 chr2:85914496-85914505 chr2:85914491-85914512
19	BHLHE40	chr2:85934409-85934783	K562	blood:	n/a	n/a
20	BHLHE40	chr2:85930244-85930301	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:85932790-85932961	K562	blood:	n/a	n/a
22	BHLHE40	chr2:85932779-85933037	HepG2	liver:	n/a	n/a
23	BHLHE40	chr2:85914370-85914640	A549	lung:	n/a	chr2:85914497-85914506 chr2:85914496-85914505 chr2:85914491-85914512
24	BHLHE40	chr2:85931853-85932480	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:85934373-85934808	GM12878	blood:	n/a	n/a
26	BRCA1	chr2:85934414-85934717	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr2:85934357-85934708	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr2:85932715-85933018	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr2:85934325-85934759	K562	blood:	n/a	n/a
30	CCNT2	chr2:85928847-85928894	K562	blood:	n/a	n/a
31	CEBPB	chr2:85932701-85933101	K562	blood:	n/a	chr2:85932894-85932905
32	CEBPB	chr2:85936547-85936699	A549	lung:	n/a	chr2:85936604-85936615
33	CEBPB	chr2:85932456-85933312	HCT-116	colon:	n/a	chr2:85932894-85932905
34	CEBPB	chr2:85932680-85933110	A549	lung:	n/a	chr2:85932894-85932905
35	CEBPB	chr2:85934617-85934622	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:85928481-85928885	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:85927910-85928111	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:85931255-85931441	HepG2	liver:	n/a	chr2:85931356-85931367
39	CEBPB	chr2:85927812-85928141	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:85931200-85931460	K562	blood:	n/a	chr2:85931356-85931367
41	CEBPB	chr2:85936441-85936752	K562	blood:	n/a	chr2:85936604-85936615
42	CEBPB	chr2:85934451-85934814	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:85932620-85933079	K562	blood:	n/a	chr2:85932894-85932905
44	CEBPB	chr2:85927889-85928096	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:85927803-85928151	A549	lung:	n/a	n/a
46	CEBPB	chr2:85914380-85914628	A549	lung:	n/a	chr2:85914519-85914532
47	CEBPB	chr2:85936452-85936781	IMR90	lung:	n/a	chr2:85936604-85936615
48	CEBPB	chr2:85936473-85936763	HepG2	liver:	n/a	chr2:85936604-85936615
49	CEBPB	chr2:85932620-85933116	HepG2	liver:	n/a	chr2:85932894-85932905
50	CEBPB	chr2:85934391-85934760	Hela-S3	cervix:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:85924685-85924735	AG09319	gingival:	n/a
2	chr2:85914525-85914575	AG04449	skin:	fetal
3	chr2:85924685-85924735	AG09319	gingival:	n/a
4	chr2:85914525-85914575	AG04449	skin:	fetal
5	chr2:85921438-85921488	HRE	kidney:	n/a
6	chr2:85921438-85921488	T-47D	breast:	n/a
7	chr2:85914525-85914575	H1-hESC	embryonic stem cell:	embryo
8	chr2:85933069-85933119	SK-N-SH_RA	brain:	n/a
9	chr2:85920000-85920050	AG04449	skin:	fetal
10	chr2:85921438-85921488	PFSK-1	brain:	n/a
11	chr2:85921963-85922013	BJ	skin:	n/a
12	chr2:85921963-85922013	HRCEpiC	kidney:	n/a
13	chr2:85921036-85921086	HCM	heart:	n/a
14	chr2:85921529-85921579	GM12891	blood:	n/a
15	chr2:85924685-85924735	H1-hESC	embryonic stem cell:	embryo
16	chr2:85925749-85925799	HRCEpiC	kidney:	n/a
17	chr2:85925749-85925799	SK-N-SH	brain:	n/a
18	chr2:85921529-85921579	NH-A	brain:	n/a
19	chr2:85914525-85914575	ECC-1	luminal epithelium:	n/a
20	chr2:85924685-85924735	NT2-D1	testis:	n/a
21	chr2:85921252-85921302	SK-N-SH_RA	brain:	n/a
22	chr2:85924685-85924735	HIPEpiC	eye:	n/a
23	chr2:85914525-85914575	HMEC	breast:	n/a
24	chr2:85925749-85925799	NB4	blood:	n/a
25	chr2:85921036-85921086	HL-60	blood:	n/a
26	chr2:85933069-85933119	H1-hESC	embryonic stem cell:	embryo
27	chr2:85921283-85921333	BJ	skin:	n/a
28	chr2:85921036-85921086	GM12891	blood:	n/a
29	chr2:85921963-85922013	T-47D	breast:	n/a
30	chr2:85924685-85924735	ECC-1	luminal epithelium:	n/a
31	chr2:85914525-85914575	AoSMC	blood vessel:	n/a
32	chr2:85914525-85914575	HL-60	blood:	n/a
33	chr2:85925749-85925799	HPAEpiC	pulmonary alveolar:	n/a
34	chr2:85914525-85914575	GM12892	blood:	n/a
35	chr2:85924685-85924735	HEK293	kidney:	embryo
36	chr2:85921252-85921302	T-47D	breast:	n/a
37	chr2:85921036-85921086	SK-N-SH_RA	brain:	n/a
38	chr2:85914525-85914575	Caco-2	colon:	n/a
39	chr2:85921529-85921579	SAEC	small airway:	n/a
40	chr2:85921252-85921302	HCT-116	colon:	n/a
41	chr2:85933069-85933119	GM19239	blood:	n/a
42	chr2:85921963-85922013	Hela-S3	cervix:	n/a
43	chr2:85914525-85914575	HEK293	kidney:	embryo
44	chr2:85925749-85925799	K562	blood:	n/a
45	chr2:85921036-85921086	CMK	blood:	n/a
46	chr2:85921438-85921488	Caco-2	colon:	n/a
47	chr2:85921252-85921302	GM06990	blood:	n/a
48	chr2:85921529-85921579	PFSK-1	brain:	n/a
49	chr2:85921529-85921579	HEK293	kidney:	embryo
50	chr2:85914525-85914575	SK-N-MC	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:85917153..85919926-chr2:85924436..85926788,2	K562	blood:
2	chr2:85939136..85942030-chr2:85944013..85946207,3	K562	blood:
3	chr2:85917153..85919926-chr2:85924436..85926788,2	K562	blood:
4	chr2:85938431..85940449-chr2:85945022..85946831,2	MCF-7	breast:
5	chr2:85906071..85907432-chr2:85933759..85935058,9	MCF-7	breast:
6	chr2:85921436..85923058-chr2:85925193..85926829,2	K562	blood:
7	chr2:85915170..85916745-chr2:85920753..85922786,2	K562	blood:
8	chr2:85930415..85932618-chr2:85965102..85967438,2	K562	blood:
9	chr2:85878852..85881419-chr2:85931468..85933087,2	MCF-7	breast:
10	chr2:85932175..85937503-chr2:85937871..85941981,7	K562	blood:
11	chr2:85924610..85926408-chr2:85954711..85957464,2	K562	blood:
12	chr2:85919636..85921243-chr2:85926613..85928346,2	MCF-7	breast:
13	chr2:85934009..85937395-chr2:85940314..85944557,5	MCF-7	breast:
14	chr2:85904933..85907760-chr2:85933076..85936019,2	MCF-7	breast:
15	chr2:85936798..85938889-chr2:85946240..85947988,2	MCF-7	breast:
16	chr2:85839135..85840661-chr2:85928083..85930394,2	MCF-7	breast:
17	chr2:85937591..85939092-chr2:85951600..85953436,2	K562	blood:
18	chr2:85905086..85909626-chr2:85912458..85918293,6	K562	blood:
19	chr2:85919636..85921243-chr2:85926613..85928346,2	MCF-7	breast:
20	chr2:85875455..85876526-chr2:85934041..85934918,4	MCF-7	breast:
21	chr2:85914382..85917156-chr2:85991881..85994505,2	MCF-7	breast:
22	chr2:85934016..85934982-chr2:85955990..85956757,2	K562	blood:
23	chr2:85912358..85914098-chr2:85920772..85923092,2	K562	blood:
24	chr2:85928909..85931848-chr2:86021884..86024213,2	K562	blood:
25	chr2:85846395..85848017-chr2:85935471..85937032,2	K562	blood:
26	chr2:85933286..85934066-chr2:86041050..86041981,2	K562	blood:
27	chr2:85932175..85937503-chr2:85937871..85941981,7	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNLY-2	chr2:85921876-85922046	NONHSAT072041
2	lnc-GNLY-2	chr2:85922027-85922309	NONHSAT072045
3	lnc-GNLY-2	chr2:85923081-85923229	NONHSAT072042
4	lnc-GNLY-2	chr2:85924111-85924800	NONHSAT072043
5	lnc-GNLY-2	chr2:85921455-85921593	NONHSAT072042
6	lnc-GNLY-2	chr2:85921465-85922546	NONHSAT072043
7	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072039
8	lnc-GNLY-2	chr2:85923081-85923617	NONHSAT072041
9	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072045
10	lnc-GNLY-2	chr2:85921549-85921593	NONHSAT072044
11	lnc-GNLY-2	chr2:85923081-85923179	NONHSAT072043
12	lnc-GNLY-1	chr2:85938746-85938850	XLOC_001556
13	lnc-SFTPB-2	chr2:85913176-85914170	NONHSAT072040
14	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072044
15	lnc-GNLY-2	chr2:85923081-85923179	NONHSAT072044
16	lnc-GNLY-2	chr2:85923081-85923853	NONHSAT072039
17	lnc-GNLY-2	chr2:85921876-85922546	NONHSAT072042
18	lnc-GNLY-2	chr2:85921451-85921593	NONHSAT072041
19	lnc-GNLY-2	chr2:85921876-85922046	NONHSAT072044
20	lnc-GNLY-2	chr2:85912298-85912344	NONHSAT072039
21	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072041
22	lnc-GNLY-2	chr2:85925687-85925870	NONHSAT072043
23	lnc-GNLY-2	chr2:85923081-85923655	NONHSAT072045
24	lnc-GNLY-2	chr2:85924111-85924224	NONHSAT072044

No data

Variant related genes	Relation type
GNLY	TF binding region
ENSG00000203363	TF binding region
GNLY	CpG island
ENSG00000203363	CpG island
ENSG00000115523	chromatin interactions
ENSG00000168883	chromatin interactions
ENSG00000203363	chromatin interactions
ENSG00000199687	chromatin interactions
ENSG00000168887	chromatin interactions

Extended variants
information (count: 1238 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6547631	chr2:85909026-85909027	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs578262625	chr2:85909094-85909095	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146071621	chr2:85909095-85909096	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs72266075	chr2:85909202-85909203	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532469327	chr2:85909203-85909204	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368849717	chr2:85909215-85909216	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190919847	chr2:85909234-85909235	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575275444	chr2:85909274-85909275	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542708942	chr2:85909326-85909327	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561177767	chr2:85909327-85909328	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs367590105	chr2:85909368-85909369	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139960294	chr2:85909373-85909374	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540841607	chr2:85909375-85909376	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs13427385	chr2:85909385-85909386	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs561866581	chr2:85909401-85909402	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs183239065	chr2:85909532-85909533	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143453789	chr2:85909540-85909541	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569668308	chr2:85909597-85909598	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs530472790	chr2:85909675-85909676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs10206742	chr2:85909691-85909692	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs541111538	chr2:85909701-85909702	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs567213369	chr2:85909703-85909704	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs534734880	chr2:85909717-85909718	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs10206759	chr2:85909731-85909732	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs571541068	chr2:85909747-85909748	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538936022	chr2:85909748-85909749	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs146761053	chr2:85909769-85909770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs533324144	chr2:85909787-85909788	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541903741	chr2:85909867-85909868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375985739	chr2:85909926-85909927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188162744	chr2:85909956-85909957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572224288	chr2:85909958-85909959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139263080	chr2:85909964-85909965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139473023	chr2:85910013-85910014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72517129	chr2:85910014-85910015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs202130784	chr2:85910040-85910041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559275241	chr2:85910041-85910042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533210754	chr2:85910045-85910046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545228985	chr2:85910050-85910051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563536553	chr2:85910062-85910063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193017260	chr2:85910078-85910079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78928147	chr2:85910096-85910097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144916840	chr2:85910097-85910098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10209258	chr2:85910133-85910134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548670597	chr2:85910225-85910226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6747600	chr2:85910407-85910408	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs142618897	chr2:85910456-85910457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546714713	chr2:85910482-85910483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571503780	chr2:85910540-85910541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150957127	chr2:85910565-85910566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
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
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:85903400-85909800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr2:85905600-85909200	Enhancers	Lung	lung
3	chr2:85905600-85909800	Enhancers	Psoas Muscle	Psoas
4	chr2:85905800-85909600	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr2:85906200-85909400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:85906400-85914000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:85906800-85909800	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr2:85906800-85911400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr2:85906800-85914400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:85906800-85918400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr2:85907400-85909200	Enhancers	Adipose Nuclei	Adipose
12	chr2:85907400-85909200	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr2:85907400-85909400	Enhancers	Left Ventricle	heart
14	chr2:85907400-85909600	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr2:85907400-85909600	Enhancers	Osteobl	bone
16	chr2:85907600-85909200	Enhancers	A549	lung
17	chr2:85908000-85909200	Enhancers	NHDF-Ad	bronchial
18	chr2:85908000-85909600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:85908000-85909600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr2:85908000-85909800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:85908000-85914800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr2:85908200-85909200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:85908200-85911600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr2:85908400-85909800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:85908400-85909800	Enhancers	Right Atrium	heart
26	chr2:85908600-85914200	Weak transcription	Brain Angular Gyrus	brain
27	chr2:85908800-85909200	Enhancers	HSMMtube	muscle
28	chr2:85908800-85909800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:85908800-85912000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr2:85908800-85914000	Weak transcription	Brain Substantia Nigra	brain
31	chr2:85908800-85914200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:85909000-85909400	Enhancers	Hela-S3	cervix
33	chr2:85909000-85914000	Weak transcription	NHLF	lung
34	chr2:85909000-85914200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr2:85909200-85913800	Weak transcription	A549	lung
36	chr2:85909200-85914200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:85909200-85921200	Weak transcription	Lung	lung
38	chr2:85909400-85911400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:85909400-85913800	Weak transcription	Hela-S3	cervix
40	chr2:85909600-85911400	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr2:85909600-85914000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:85909600-85914200	Weak transcription	Osteobl	bone
43	chr2:85909800-85911600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr2:85909800-85911800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr2:85909800-85914000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr2:85909800-85914200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr2:85909800-85914600	Weak transcription	Psoas Muscle	Psoas
48	chr2:85909800-85920800	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr2:85911400-85912000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr2:85911400-85912200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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