Variant report

Variant	nsv1038498
Chromosome Location	chr12:44679455-44816572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:44799010-44799377	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:44693354-44693558	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr12:44798931-44799339	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr12:44797015-44797309	GM12878	blood:	n/a	chr12:44797156-44797167
5	BATF	chr12:44732733-44733024	GM12878	blood:	n/a	n/a
6	BATF	chr12:44680163-44680412	GM12878	blood:	n/a	chr12:44680268-44680278 chr12:44680267-44680278
7	BATF	chr12:44688366-44688681	GM12878	blood:	n/a	n/a
8	BATF	chr12:44680181-44680366	GM12878	blood:	n/a	chr12:44680268-44680278 chr12:44680267-44680278
9	BCL11A	chr12:44680182-44680482	GM12878	blood:	n/a	chr12:44680270-44680279
10	BCL11A	chr12:44680144-44680389	GM12878	blood:	n/a	chr12:44680270-44680279
11	BHLHE40	chr12:44688576-44688828	GM12878	blood:	n/a	n/a
12	CEBPB	chr12:44681380-44681682	IMR90	lung:	n/a	n/a
13	CEBPB	chr12:44800895-44801073	H1-hESC	embryonic stem cell:	n/a	chr12:44800986-44800997
14	CEBPB	chr12:44711143-44711271	H1-hESC	embryonic stem cell:	n/a	chr12:44711233-44711244
15	CEBPB	chr12:44752533-44752829	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:44779901-44780057	A549	lung:	n/a	chr12:44779980-44779991
17	CEBPB	chr12:44690075-44690381	HepG2	liver:	n/a	chr12:44690209-44690220
18	CEBPB	chr12:44711249-44711304	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:44779832-44780077	HepG2	liver:	n/a	chr12:44779980-44779991
20	CEBPB	chr12:44738424-44738774	HepG2	liver:	n/a	chr12:44738465-44738478 chr12:44738448-44738461
21	CEBPB	chr12:44800814-44801161	IMR90	lung:	n/a	chr12:44800986-44800997
22	CEBPB	chr12:44800833-44801170	HepG2	liver:	n/a	chr12:44800986-44800997
23	CEBPB	chr12:44800949-44801062	K562	blood:	n/a	chr12:44800986-44800997
24	CEBPB	chr12:44752531-44752846	A549	lung:	n/a	n/a
25	CEBPB	chr12:44710298-44710883	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:44800876-44801153	A549	lung:	n/a	chr12:44800986-44800997
27	CEBPZ	chr12:44770594-44770669	HepG2	liver:	n/a	n/a
28	CTCF	chr12:44711739-44711844	ProgFib	skin:	n/a	n/a
29	CTCF	chr12:44711393-44711633	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr12:44800652-44800781	LNCaP	prostate:	n/a	n/a
31	CTCF	chr12:44711440-44711590	HCM	heart:	n/a	n/a
32	CTCF	chr12:44779380-44779530	Caco-2	colon:	n/a	n/a
33	CTCF	chr12:44711780-44711930	AG04449	skin:	n/a	n/a
34	CTCF	chr12:44711480-44711630	BJ	skin:	n/a	n/a
35	CTCF	chr12:44784004-44784066	LNCaP	prostate:	n/a	n/a
36	CTCF	chr12:44711440-44711590	Caco-2	colon:	n/a	n/a
37	CTCF	chr12:44711400-44711550	HFF	foreskin:	n/a	n/a
38	CTCF	chr12:44711420-44711570	GM12864	blood:	n/a	n/a
39	CTCF	chr12:44711860-44712010	GM12865	blood:	n/a	n/a
40	CTCF	chr12:44711619-44711821	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:44711377-44711636	A549	lung:	n/a	n/a
42	CTCF	chr12:44711409-44711796	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:44711385-44711809	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:44711402-44711646	GM19239	blood:	n/a	n/a
45	CTCF	chr12:44711460-44711610	GM12870	blood:	n/a	n/a
46	CTCF	chr12:44711412-44711661	T-47D	breast:	n/a	n/a
47	CTCF	chr12:44711440-44711590	GM12873	blood:	n/a	n/a
48	CTCF	chr12:44800620-44800770	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr12:44711680-44711830	GM12871	blood:	n/a	n/a
50	CTCF	chr12:44711234-44711910	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:44782459-44782509	HCPEpiC	choroid plexus:	n/a
2	chr12:44775162-44775212	ProgFib	skin:	n/a
3	chr12:44775162-44775212	CMK	blood:	n/a
4	chr12:44782459-44782509	AG09319	gingival:	n/a
5	chr12:44782459-44782509	NT2-D1	testis:	n/a
6	chr12:44775162-44775212	AG04449	skin:	fetal
7	chr12:44782459-44782509	PANC-1	pancreas:	n/a
8	chr12:44782459-44782509	T-47D	breast:	n/a
9	chr12:44782459-44782509	GM12891	blood:	n/a
10	chr12:44782459-44782509	H1-hESC	embryonic stem cell:	embryo
11	chr12:44775162-44775212	GM12892	blood:	n/a
12	chr12:44775162-44775212	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:44782459-44782509	HAEpiC	amniotic membrane:	n/a
14	chr12:44782459-44782509	GM19239	blood:	n/a
15	chr12:44775162-44775212	SK-N-SH	brain:	n/a
16	chr12:44782459-44782509	HCT-116	colon:	n/a
17	chr12:44775162-44775212	BE2_C	brain:	n/a
18	chr12:44775162-44775212	HUVEC	blood vessel:	n/a
19	chr12:44775162-44775212	U87	brain:	n/a
20	chr12:44782459-44782509	HCF	heart:	n/a
21	chr12:44782459-44782509	HRPEpiC	eye:	n/a
22	chr12:44775162-44775212	HCF	heart:	n/a
23	chr12:44775162-44775212	Jurkat	blood:	n/a
24	chr12:44775162-44775212	NT2-D1	testis:	n/a
25	chr12:44782459-44782509	SK-N-MC	brain:	n/a
26	chr12:44775162-44775212	HIPEpiC	eye:	n/a
27	chr12:44782459-44782509	AG09309	skin:	n/a
28	chr12:44775162-44775212	RPTEC	kidney:	n/a
29	chr12:44775162-44775212	SK-N-MC	brain:	n/a
30	chr12:44782459-44782509	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:44775162-44775212	NHBE	bronchial:	n/a
32	chr12:44775162-44775212	NHDF-neo	bronchial:	n/a
33	chr12:44782459-44782509	SK-N-SH	brain:	n/a
34	chr12:44775162-44775212	HRCEpiC	kidney:	n/a
35	chr12:44782459-44782509	ovcar-3	ovarian:	n/a
36	chr12:44782459-44782509	PrEC	prostate:	n/a
37	chr12:44782459-44782509	GM12878	blood:	n/a
38	chr12:44782459-44782509	Caco-2	colon:	n/a
39	chr12:44782459-44782509	HCM	heart:	n/a
40	chr12:44775162-44775212	HepG2	liver:	n/a
41	chr12:44782459-44782509	HIPEpiC	eye:	n/a
42	chr12:44782459-44782509	IMR90	lung:	fetal
43	chr12:44782459-44782509	AG04450	lung:	fetal
44	chr12:44775162-44775212	SAEC	small airway:	n/a
45	chr12:44775162-44775212	BJ	skin:	n/a
46	chr12:44775162-44775212	ECC-1	luminal epithelium:	n/a
47	chr12:44775162-44775212	MCF-7	breast:	n/a
48	chr12:44782459-44782509	HEK293	kidney:	embryo
49	chr12:44782459-44782509	NHDF-neo	bronchial:	n/a
50	chr12:44775162-44775212	HCPEpiC	choroid plexus:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:44793231..44794791-chr12:44901498..44904430,2	MCF-7	breast:
2	chr12:44808565..44810933-chr12:44813999..44816654,2	MCF-7	breast:
3	chr12:44755908..44757625-chr12:44780737..44782461,2	MCF-7	breast:
4	chr12:44802428..44804670-chr12:44804925..44807646,2	K562	blood:
5	chr12:44763525..44765567-chr12:44767593..44769212,2	K562	blood:
6	chr12:44808565..44810933-chr12:44813999..44816654,2	MCF-7	breast:
7	chr12:44778148..44778873-chr12:127671997..127672597,2	K562	blood:
8	chr12:44710214..44712125-chr12:44712657..44715022,2	MCF-7	breast:
9	chr12:44773541..44775269-chr12:44780927..44783854,2	MCF-7	breast:
10	chr12:44755908..44757625-chr12:44780737..44782461,2	MCF-7	breast:
11	chr12:44802428..44804670-chr12:44804925..44807646,2	K562	blood:
12	chr12:44782966..44785826-chr12:44799216..44800992,2	MCF-7	breast:
13	chr12:44773541..44775269-chr12:44780927..44783854,2	MCF-7	breast:
14	chr12:44763525..44765567-chr12:44767593..44769212,2	K562	blood:
15	chr12:44782966..44785826-chr12:44799216..44800992,2	MCF-7	breast:
16	chr12:44771877..44773660-chr12:44776294..44779206,2	K562	blood:
17	chr12:44771877..44773660-chr12:44776294..44779206,2	K562	blood:

No data

Variant related genes	Relation type
TMEM117	TF binding region
TMEM117	CpG island
ENSG00000139173	chromatin interactions

Extended variants
information (count: 4512 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:4512 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373360982	chr12:44679510-44679511	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs568157982	chr12:44679516-44679517	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs529026250	chr12:44679518-44679519	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs191401143	chr12:44679617-44679618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17094384	chr12:44679637-44679638	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183463603	chr12:44679698-44679699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144920157	chr12:44679773-44679774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570470044	chr12:44679830-44679831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570449713	chr12:44679831-44679832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537836304	chr12:44679849-44679850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556189037	chr12:44679866-44679867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375148889	chr12:44679907-44679908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574573058	chr12:44679936-44679937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149027448	chr12:44679988-44679989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187952823	chr12:44679991-44679992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73086772	chr12:44680061-44680062	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545733270	chr12:44680072-44680073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564382115	chr12:44680168-44680169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372530227	chr12:44680175-44680176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142042890	chr12:44680187-44680188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192766541	chr12:44680190-44680191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183681400	chr12:44680241-44680242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562333303	chr12:44680256-44680257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377751682	chr12:44680308-44680309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537723211	chr12:44680325-44680326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566903345	chr12:44680394-44680395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186528130	chr12:44680430-44680431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374257359	chr12:44680453-44680454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552535395	chr12:44680530-44680531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192526182	chr12:44680566-44680567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17094386	chr12:44680581-44680582	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs151175004	chr12:44680647-44680648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74084469	chr12:44680654-44680655	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1798027	chr12:44680713-44680714	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184524616	chr12:44680719-44680720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190418566	chr12:44680803-44680804	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141180816	chr12:44680833-44680834	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558011166	chr12:44680835-44680836	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534457207	chr12:44680839-44680840	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73274199	chr12:44680847-44680848	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs77501018	chr12:44680872-44680873	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574606361	chr12:44680925-44680926	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146985772	chr12:44680935-44680936	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540727277	chr12:44680945-44680946	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181694523	chr12:44680962-44680963	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185019309	chr12:44680980-44680981	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189485568	chr12:44680996-44680997	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529531372	chr12:44681008-44681009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17094396	chr12:44681022-44681023	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs61933049	chr12:44681028-44681029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44672800-44680600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:44676600-44680400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:44676600-44697800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:44678000-44680600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:44678800-44679600	Enhancers	Colon Smooth Muscle	Colon
6	chr12:44678800-44679600	Enhancers	Fetal Brain Female	brain
7	chr12:44679000-44679600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:44679000-44679600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
9	chr12:44679000-44679600	Enhancers	Fetal Brain Male	brain
10	chr12:44679000-44680600	Enhancers	HUVEC	blood vessel
11	chr12:44679000-44680800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:44679200-44679600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr12:44679200-44679600	Enhancers	Esophagus	oesophagus
14	chr12:44679200-44679600	Enhancers	Gastric	stomach
15	chr12:44679200-44679600	Enhancers	Psoas Muscle	Psoas
16	chr12:44679200-44680800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr12:44679200-44682000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr12:44679400-44679600	Enhancers	Pancreas	Pancrea
19	chr12:44679400-44681400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr12:44679400-44681600	Enhancers	HSMM	muscle
21	chr12:44679600-44679800	Enhancers	NHDF-Ad	bronchial
22	chr12:44679600-44680000	Weak transcription	Fetal Brain Male	brain
23	chr12:44679600-44680600	Weak transcription	Fetal Brain Female	brain
24	chr12:44679600-44681800	Enhancers	NHEK	skin
25	chr12:44679800-44680600	Weak transcription	NHDF-Ad	bronchial
26	chr12:44680000-44680800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:44680000-44681200	Enhancers	Fetal Brain Male	brain
28	chr12:44680200-44681600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr12:44680200-44682000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr12:44680400-44682000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:44680400-44682000	Enhancers	HMEC	breast
32	chr12:44680600-44681000	Enhancers	Brain Germinal Matrix	brain
33	chr12:44680600-44681200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:44680600-44681400	Enhancers	NH-A	brain
35	chr12:44680600-44681400	Enhancers	NHDF-Ad	bronchial
36	chr12:44680600-44681600	Enhancers	Fetal Brain Female	brain
37	chr12:44680600-44681800	Enhancers	Osteobl	bone
38	chr12:44680600-44682000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:44680800-44681000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:44681000-44682000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:44681200-44681800	Weak transcription	Fetal Brain Male	brain
42	chr12:44681200-44684000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:44681800-44682000	Enhancers	Fetal Brain Male	brain
44	chr12:44682000-44698600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:44684000-44685000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:44685000-44695400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:44688000-44688400	Enhancers	GM12878-XiMat	blood
48	chr12:44688000-44689400	Enhancers	Primary B cells from peripheral blood	blood
49	chr12:44688400-44688800	Flanking Active TSS	GM12878-XiMat	blood
50	chr12:44688600-44688800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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