Variant report

Variant	nsv583294
Chromosome Location	chr2:151022044-151037893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:151022952-151023612	K562	blood:	n/a	n/a
2	ARID3A	chr2:151024237-151024609	K562	blood:	n/a	n/a
3	ARID3A	chr2:151026490-151026497	K562	blood:	n/a	n/a
4	ATF1	chr2:151022603-151023539	K562	blood:	n/a	n/a
5	ATF1	chr2:151028405-151028790	K562	blood:	n/a	n/a
6	ATF1	chr2:151035039-151035302	K562	blood:	n/a	n/a
7	ATF1	chr2:151024125-151024512	K562	blood:	n/a	n/a
8	ATF1	chr2:151024719-151024883	K562	blood:	n/a	n/a
9	ATF2	chr2:151024160-151024558	GM12878	blood:	n/a	n/a
10	ATF2	chr2:151024180-151024606	GM12878	blood:	n/a	n/a
11	ATF3	chr2:151024101-151024534	K562	blood:	n/a	n/a
12	ATF3	chr2:151022648-151023351	A549	lung:	n/a	n/a
13	ATF3	chr2:151022564-151023322	A549	lung:	n/a	n/a
14	BACH1	chr2:151022971-151023283	K562	blood:	n/a	n/a
15	BATF	chr2:151024093-151024518	GM12878	blood:	n/a	chr2:151024332-151024342 chr2:151024331-151024342 chr2:151024328-151024338
16	BATF	chr2:151024149-151024506	GM12878	blood:	n/a	chr2:151024332-151024342 chr2:151024331-151024342 chr2:151024328-151024338
17	BCL11A	chr2:151024113-151024507	GM12878	blood:	n/a	chr2:151024331-151024340 chr2:151024330-151024339
18	BCL3	chr2:151024112-151024796	A549	lung:	n/a	chr2:151024331-151024340 chr2:151024330-151024339
19	BCL3	chr2:151022597-151023297	A549	lung:	n/a	n/a
20	BCL3	chr2:151022607-151023328	A549	lung:	n/a	n/a
21	BHLHE40	chr2:151024223-151024459	K562	blood:	n/a	n/a
22	BHLHE40	chr2:151026203-151026254	K562	blood:	n/a	n/a
23	BHLHE40	chr2:151024257-151024555	GM12878	blood:	n/a	n/a
24	BHLHE40	chr2:151022684-151022862	K562	blood:	n/a	n/a
25	CBX3	chr2:151022715-151023222	K562	blood:	n/a	n/a
26	CCNT2	chr2:151023011-151023488	K562	blood:	n/a	n/a
27	CEBPB	chr2:151022536-151022849	ECC-1	luminal epithelium:	n/a	chr2:151022687-151022698
28	CEBPB	chr2:151025407-151026111	A549	lung:	n/a	chr2:151025439-151025450
29	CEBPB	chr2:151024168-151024711	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr2:151034966-151035444	A549	lung:	n/a	n/a
31	CEBPB	chr2:151022521-151022872	IMR90	lung:	n/a	chr2:151022687-151022698
32	CEBPB	chr2:151022587-151022811	K562	blood:	n/a	chr2:151022687-151022698
33	CEBPB	chr2:151022542-151023256	A549	lung:	n/a	chr2:151022687-151022698
34	CEBPB	chr2:151022512-151022873	HepG2	liver:	n/a	chr2:151022687-151022698
35	CEBPB	chr2:151024162-151024805	A549	lung:	n/a	n/a
36	CEBPB	chr2:151034980-151035502	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr2:151025258-151025627	A549	lung:	n/a	chr2:151025439-151025450
38	CEBPB	chr2:151022487-151023215	Hela-S3	cervix:	n/a	chr2:151022687-151022698
39	CEBPB	chr2:151022480-151023075	HCT-116	colon:	n/a	chr2:151022687-151022698
40	CEBPB	chr2:151035131-151035201	A549	lung:	n/a	n/a
41	CEBPB	chr2:151022292-151023149	A549	lung:	n/a	chr2:151022687-151022698
42	CEBPB	chr2:151022465-151023126	HCT-116	colon:	n/a	chr2:151022687-151022698
43	CEBPB	chr2:151022481-151022854	K562	blood:	n/a	chr2:151022687-151022698
44	CEBPB	chr2:151034990-151035488	MCF-7	breast:	n/a	n/a
45	CEBPB	chr2:151022488-151023048	K562	blood:	n/a	chr2:151022687-151022698
46	CEBPB	chr2:151022550-151022927	ECC-1	luminal epithelium:	n/a	chr2:151022687-151022698
47	CEBPB	chr2:151035071-151035430	MCF-7	breast:	n/a	n/a
48	CEBPB	chr2:151024113-151024668	MCF-7	breast:	n/a	n/a
49	CEBPB	chr2:151025024-151025553	MCF-7	breast:	n/a	chr2:151025439-151025450
50	CEBPB	chr2:151022444-151023528	A549	lung:	n/a	chr2:151022687-151022698

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:151027710-151027760	HCM	heart:	n/a
2	chr2:151027710-151027760	GM12891	blood:	n/a
3	chr2:151025188-151025238	HAEpiC	amniotic membrane:	n/a
4	chr2:151025188-151025238	GM12891	blood:	n/a
5	chr2:151027710-151027760	NB4	blood:	n/a
6	chr2:151025188-151025238	HCF	heart:	n/a
7	chr2:151025188-151025238	GM12878	blood:	n/a
8	chr2:151025188-151025238	K562	blood:	n/a
9	chr2:151027710-151027760	IMR90	lung:	fetal
10	chr2:151025188-151025238	HepG2	liver:	n/a
11	chr2:151025188-151025238	SKMC	muscle:	n/a
12	chr2:151027710-151027760	PANC-1	pancreas:	n/a
13	chr2:151027710-151027760	PFSK-1	brain:	n/a
14	chr2:151027710-151027760	MCF10A-Er-Src	breast:	n/a
15	chr2:151025188-151025238	CMK	blood:	n/a
16	chr2:151027710-151027760	AoSMC	blood vessel:	n/a
17	chr2:151027710-151027760	HEEpiC	esophagus:	n/a
18	chr2:151027710-151027760	SK-N-SH_RA	brain:	n/a
19	chr2:151027710-151027760	GM19239	blood:	n/a
20	chr2:151025188-151025238	SK-N-SH	brain:	n/a
21	chr2:151027710-151027760	HNPCEpiC	eye:	n/a
22	chr2:151025188-151025238	PFSK-1	brain:	n/a
23	chr2:151025188-151025238	U87	brain:	n/a
24	chr2:151027710-151027760	ovcar-3	ovarian:	n/a
25	chr2:151027710-151027760	NHDF-neo	bronchial:	n/a
26	chr2:151025188-151025238	HNPCEpiC	eye:	n/a
27	chr2:151025188-151025238	HEK293	kidney:	embryo
28	chr2:151027710-151027760	NHBE	bronchial:	n/a
29	chr2:151025188-151025238	HMEC	breast:	n/a
30	chr2:151025188-151025238	SK-N-SH_RA	brain:	n/a
31	chr2:151025188-151025238	GM19239	blood:	n/a
32	chr2:151027710-151027760	Hepatocyte	liver:	n/a
33	chr2:151027710-151027760	GM12892	blood:	n/a
34	chr2:151025188-151025238	RPTEC	kidney:	n/a
35	chr2:151025188-151025238	PANC-1	pancreas:	n/a
36	chr2:151025188-151025238	GM12892	blood:	n/a
37	chr2:151027710-151027760	K562	blood:	n/a
38	chr2:151027710-151027760	SK-N-SH	brain:	n/a
39	chr2:151027710-151027760	CMK	blood:	n/a
40	chr2:151027710-151027760	HAEpiC	amniotic membrane:	n/a
41	chr2:151027710-151027760	HUVEC	blood vessel:	n/a
42	chr2:151027710-151027760	AG09309	skin:	n/a
43	chr2:151027710-151027760	LNCaP	prostate:	n/a
44	chr2:151027710-151027760	HL-60	blood:	n/a
45	chr2:151025188-151025238	NT2-D1	testis:	n/a
46	chr2:151027710-151027760	HMEC	breast:	n/a
47	chr2:151027710-151027760	T-47D	breast:	n/a
48	chr2:151027710-151027760	SAEC	small airway:	n/a
49	chr2:151025188-151025238	GM06990	blood:	n/a
50	chr2:151025188-151025238	A549	lung:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:151024105..151026870-chr2:151120233..151122729,2	MCF-7	breast:
2	chr2:151018984..151021461-chr2:151021617..151024029,2	K562	blood:
3	chr2:151019127..151021972-chr2:151024346..151026624,2	K562	blood:
4	chr2:151015440..151017637-chr2:151020964..151024352,3	MCF-7	breast:
5	chr2:150988564..150990849-chr2:151022615..151025266,3	MCF-7	breast:
6	chr2:151015327..151017230-chr2:151030179..151032620,2	K562	blood:
7	chr2:150848914..150851850-chr2:151022945..151025102,2	MCF-7	breast:
8	chr2:151025085..151027146-chr2:151027265..151029673,2	MCF-7	breast:
9	chr2:151018212..151020426-chr2:151020566..151023225,3	MCF-7	breast:
10	chr2:151020603..151025476-chr2:151341674..151344465,7	MCF-7	breast:
11	chr2:151015971..151018361-chr2:151021107..151023162,2	K562	blood:
12	chr2:151022613..151024999-chr2:151332492..151334061,2	MCF-7	breast:
13	chr2:151021749..151023909-chr2:151069571..151071445,2	MCF-7	breast:
14	chr2:151022947..151025702-chr2:151341739..151344961,4	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RND3-4	chr2:151022596-151022842	XLOC_002353
2	lnc-LYPD6-3	chr2:151026010-151026153	XLOC_001704
3	lnc-LYPD6-3	chr2:151026002-151026455	NONHSAT074918

No data

Variant related genes	Relation type
ENSG00000230645	TF binding region
ENSG00000230645	CpG island
ENSG00000230645	chromatin interactions
ENSG00000115963	chromatin interactions
GNAS	miRNA target sites

Extended variants
information (count: 576 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:576 , 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	rs10178850	chr2:151022044-151022045	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186527395	chr2:151022050-151022051	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567661695	chr2:151022082-151022083	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538148344	chr2:151022085-151022086	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557375552	chr2:151022094-151022095	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191917514	chr2:151022115-151022116	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536767185	chr2:151022174-151022175	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112722899	chr2:151022183-151022184	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs12618290	chr2:151022218-151022219	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs545227405	chr2:151022230-151022231	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs559249909	chr2:151022274-151022275	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143855139	chr2:151022285-151022286	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs116120305	chr2:151022378-151022379	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs183914522	chr2:151022458-151022459	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs80049110	chr2:151022492-151022493	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186856563	chr2:151022498-151022499	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558975428	chr2:151022543-151022544	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562504263	chr2:151022545-151022546	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528332894	chr2:151022602-151022603	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs2376606	chr2:151022637-151022638	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs368322821	chr2:151022653-151022654	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs114040006	chr2:151022679-151022680	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs571549451	chr2:151022682-151022683	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs145714950	chr2:151022686-151022687	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs550867982	chr2:151022724-151022725	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs115139974	chr2:151022755-151022756	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs536609695	chr2:151022767-151022768	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs954077	chr2:151022786-151022787	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566851843	chr2:151022863-151022864	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539264256	chr2:151022883-151022884	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191650354	chr2:151022892-151022893	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575923869	chr2:151023038-151023039	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs113097608	chr2:151023055-151023056	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561639665	chr2:151023080-151023081	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549004899	chr2:151023096-151023097	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554799389	chr2:151023121-151023122	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs143722647	chr2:151023300-151023301	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs151057845	chr2:151023346-151023347	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182565885	chr2:151023356-151023357	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572835509	chr2:151023367-151023368	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs545215468	chr2:151023406-151023407	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs78944025	chr2:151023429-151023430	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530690037	chr2:151023491-151023492	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377552962	chr2:151023519-151023520	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs141372435	chr2:151023542-151023543	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530164075	chr2:151023563-151023564	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531771361	chr2:151023623-151023624	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566990917	chr2:151023699-151023700	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538738392	chr2:151023739-151023740	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs377094448	chr2:151023766-151023767	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	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
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151013400-151023800	Weak transcription	Fetal Brain Male	brain
2	chr2:151013800-151022800	Weak transcription	Fetal Lung	lung
3	chr2:151017200-151024000	Weak transcription	NHDF-Ad	bronchial
4	chr2:151018600-151022800	Weak transcription	Aorta	Aorta
5	chr2:151019400-151022600	Weak transcription	Fetal Muscle Leg	muscle
6	chr2:151020200-151022600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:151020400-151022600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:151020400-151022600	Weak transcription	Brain Germinal Matrix	brain
9	chr2:151020400-151022600	Weak transcription	HUVEC	blood vessel
10	chr2:151021400-151022400	Enhancers	A549	lung
11	chr2:151021600-151023200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:151021800-151023200	Enhancers	Stomach Smooth Muscle	stomach
13	chr2:151021800-151023400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr2:151021800-151023400	Enhancers	Colon Smooth Muscle	Colon
15	chr2:151021800-151026200	Enhancers	NH-A	brain
16	chr2:151021800-151026800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:151022000-151022200	Flanking Active TSS	Liver	Liver
18	chr2:151022000-151022800	Enhancers	K562	blood
19	chr2:151022000-151023600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:151022200-151022400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:151022200-151022600	Enhancers	Hela-S3	cervix
22	chr2:151022200-151023000	Active TSS	Liver	Liver
23	chr2:151022200-151026000	Enhancers	HMEC	breast
24	chr2:151022200-151026400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr2:151022200-151026400	Enhancers	Osteobl	bone
26	chr2:151022400-151023000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr2:151022400-151023600	Flanking Active TSS	A549	lung
28	chr2:151022600-151022800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:151022600-151023000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr2:151022600-151023000	Enhancers	Psoas Muscle	Psoas
31	chr2:151022600-151023200	Enhancers	Fetal Muscle Leg	muscle
32	chr2:151022600-151023200	Enhancers	Pancreas	Pancrea
33	chr2:151022600-151023200	Enhancers	Rectal Smooth Muscle	rectum
34	chr2:151022600-151023200	Flanking Active TSS	Hela-S3	cervix
35	chr2:151022600-151023200	Enhancers	NHLF	lung
36	chr2:151022600-151023400	Enhancers	Brain Germinal Matrix	brain
37	chr2:151022600-151024800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr2:151022600-151025400	Enhancers	HUVEC	blood vessel
39	chr2:151022600-151025400	Enhancers	NHEK	skin
40	chr2:151022600-151025800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:151022600-151026400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr2:151022800-151023000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:151022800-151023000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr2:151022800-151023000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:151022800-151023000	Enhancers	Stomach Mucosa	stomach
46	chr2:151022800-151023200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr2:151022800-151023200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:151022800-151023200	Enhancers	Aorta	Aorta
49	chr2:151022800-151023200	Enhancers	Esophagus	oesophagus
50	chr2:151022800-151023200	Enhancers	Fetal Lung	lung

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