Variant report

Variant	nsv1044694
Chromosome Location	chr12:63746069-63920831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:650)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:63813947-63814280	K562	blood:	n/a	n/a
2	ATF1	chr12:63874624-63874684	K562	blood:	n/a	n/a
3	BACH1	chr12:63835477-63835549	K562	blood:	n/a	n/a
4	BATF	chr12:63812966-63813225	GM12878	blood:	n/a	chr12:63813058-63813069 chr12:63813086-63813097 chr12:63813114-63813125
5	CBX3	chr12:63813973-63814373	K562	blood:	n/a	n/a
6	CBX3	chr12:63812790-63813727	HCT-116	colon:	n/a	n/a
7	CBX3	chr12:63813979-63814307	K562	blood:	n/a	n/a
8	CBX3	chr12:63812814-63813379	HCT-116	colon:	n/a	n/a
9	CEBPB	chr12:63748967-63749256	A549	lung:	n/a	chr12:63749160-63749171
10	CEBPB	chr12:63839798-63840058	IMR90	lung:	n/a	chr12:63839911-63839922
11	CEBPB	chr12:63839778-63840018	HepG2	liver:	n/a	chr12:63839911-63839922
12	CEBPB	chr12:63839788-63839947	H1-hESC	embryonic stem cell:	n/a	chr12:63839911-63839922
13	CEBPB	chr12:63916532-63916622	A549	lung:	n/a	chr12:63916575-63916586
14	CEBPB	chr12:63916557-63916595	HepG2	liver:	n/a	chr12:63916575-63916586
15	CEBPB	chr12:63794562-63794848	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:63749118-63749197	HepG2	liver:	n/a	chr12:63749160-63749171
17	CEBPB	chr12:63787481-63787733	HepG2	liver:	n/a	n/a
18	CHD1	chr12:63809442-63809729	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr12:63793910-63793913	HepG2	liver:	n/a	n/a
20	CHD2	chr12:63814034-63814237	K562	blood:	n/a	n/a
21	CTCF	chr12:63814040-63814190	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr12:63814000-63814150	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr12:63747380-63747530	HBMEC	blood vessel:	n/a	chr12:63747489-63747510 chr12:63747490-63747499
24	CTCF	chr12:63813955-63814324	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:63813980-63814130	NHEK	skin:	n/a	n/a
26	CTCF	chr12:63887220-63887370	HepG2	liver:	n/a	n/a
27	CTCF	chr12:63814010-63814197	GM12891	blood:	n/a	n/a
28	CTCF	chr12:63814400-63814550	AG04450	lung:	n/a	n/a
29	CTCF	chr12:63886938-63887017	Medullo	brain:	n/a	n/a
30	CTCF	chr12:63814000-63814150	HCFaa	heart:	n/a	n/a
31	CTCF	chr12:63868222-63868310	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:63814000-63814150	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:63813980-63814130	HMEC	breast:	n/a	n/a
34	CTCF	chr12:63814020-63814170	GM12864	blood:	n/a	n/a
35	CTCF	chr12:63813980-63814130	NB4	blood:	n/a	n/a
36	CTCF	chr12:63814000-63814173	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr12:63747466-63747559	LNCaP	prostate:	n/a	chr12:63747489-63747510 chr12:63747490-63747499
38	CTCF	chr12:63814000-63814150	GM06990	blood:	n/a	n/a
39	CTCF	chr12:63814040-63814190	GM12871	blood:	n/a	n/a
40	CTCF	chr12:63813958-63814251	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:63814040-63814190	GM12865	blood:	n/a	n/a
42	CTCF	chr12:63852767-63852904	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr12:63813940-63814090	HAc	cerebellar:	n/a	n/a
44	CTCF	chr12:63813940-63814090	HFF	foreskin:	n/a	n/a
45	CTCF	chr12:63814020-63814170	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr12:63868260-63868410	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:63813980-63814130	AG04450	lung:	n/a	n/a
48	CTCF	chr12:63814020-63814170	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr12:63747440-63747590	HBMEC	blood vessel:	n/a	chr12:63747489-63747510 chr12:63747490-63747499
50	CTCF	chr12:63813980-63814130	GM12867	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63754169-63754219	HCPEpiC	choroid plexus:	n/a
2	chr12:63754169-63754219	IMR90	lung:	fetal
3	chr12:63754169-63754219	NHBE	bronchial:	n/a
4	chr12:63754169-63754219	HepG2	liver:	n/a
5	chr12:63754169-63754219	HL-60	blood:	n/a
6	chr12:63754169-63754219	ECC-1	luminal epithelium:	n/a
7	chr12:63754169-63754219	HEEpiC	esophagus:	n/a
8	chr12:63754169-63754219	MCF-7	breast:	n/a
9	chr12:63754169-63754219	PrEC	prostate:	n/a
10	chr12:63754169-63754219	AG09309	skin:	n/a
11	chr12:63754169-63754219	Hepatocyte	liver:	n/a
12	chr12:63754169-63754219	HRE	kidney:	n/a
13	chr12:63754169-63754219	Hela-S3	cervix:	n/a
14	chr12:63754169-63754219	HUVEC	blood vessel:	n/a
15	chr12:63754169-63754219	LNCaP	prostate:	n/a
16	chr12:63754169-63754219	GM06990	blood:	n/a
17	chr12:63754169-63754219	SK-N-SH	brain:	n/a
18	chr12:63754169-63754219	HEK293	kidney:	embryo
19	chr12:63754169-63754219	Caco-2	colon:	n/a
20	chr12:63754169-63754219	SKMC	muscle:	n/a
21	chr12:63754169-63754219	HRPEpiC	eye:	n/a
22	chr12:63754169-63754219	GM12892	blood:	n/a
23	chr12:63754169-63754219	CMK	blood:	n/a
24	chr12:63754169-63754219	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:63754169-63754219	BJ	skin:	n/a
26	chr12:63754169-63754219	HMEC	breast:	n/a
27	chr12:63754169-63754219	HCF	heart:	n/a
28	chr12:63754169-63754219	AG10803	skin:	n/a
29	chr12:63754169-63754219	Jurkat	blood:	n/a
30	chr12:63754169-63754219	RPTEC	kidney:	n/a
31	chr12:63754169-63754219	HCT-116	colon:	n/a
32	chr12:63754169-63754219	AG04450	lung:	fetal
33	chr12:63754169-63754219	GM12878	blood:	n/a
34	chr12:63754169-63754219	U87	brain:	n/a
35	chr12:63754169-63754219	NH-A	brain:	n/a
36	chr12:63754169-63754219	ovcar-3	ovarian:	n/a
37	chr12:63754169-63754219	HAEpiC	amniotic membrane:	n/a
38	chr12:63754169-63754219	HCM	heart:	n/a
39	chr12:63754169-63754219	BE2_C	brain:	n/a
40	chr12:63754169-63754219	HIPEpiC	eye:	n/a
41	chr12:63754169-63754219	ProgFib	skin:	n/a
42	chr12:63754169-63754219	NHDF-neo	bronchial:	n/a
43	chr12:63754169-63754219	MCF10A-Er-Src	breast:	n/a
44	chr12:63754169-63754219	SAEC	small airway:	n/a
45	chr12:63754169-63754219	PANC-1	pancreas:	n/a
46	chr12:63754169-63754219	AG09319	gingival:	n/a
47	chr12:63754169-63754219	GM12891	blood:	n/a
48	chr12:63754169-63754219	GM19239	blood:	n/a
49	chr12:63754169-63754219	AoSMC	blood vessel:	n/a
50	chr12:63754169-63754219	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:63893978..63896181-chr12:64171241..64172887,2	K562	blood:
2	chr12:63743207..63745868-chr12:63754623..63756737,2	K562	blood:
3	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:
4	chr12:63813649..63814184-chr12:64195525..64196396,2	K562	blood:
5	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
6	chr12:63768242..63768742-chr9:139887190..139887694,2	Hela-S3	cervix:
7	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:
8	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
9	chr12:63842271..63844496-chr12:63846747..63849454,2	MCF-7	breast:
10	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:
11	chr12:63799854..63801447-chr12:63805061..63807630,2	MCF-7	breast:
12	chr12:63808447..63811341-chr3:64933107..64935525,2	MCF-7	breast:
13	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
14	chr12:63793684..63795622-chr12:63796848..63799129,2	K562	blood:
15	chr12:63902632..63905089-chr12:63908351..63910373,2	MCF-7	breast:
16	chr12:63912615..63915340-chr12:63916183..63918806,2	K562	blood:
17	chr12:63779288..63781863-chr12:63785380..63788131,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVPR1A-1	chr12:63753656-63753817	ENSG00000258117

No data

Variant related genes	Relation type
ENSG00000258117	TF binding region
ENSG00000258117	CpG island
ENSG00000148362	chromatin interactions

Extended variants
information (count: 3389 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3389 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576095171	chr12:63746070-63746071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149848187	chr12:63746135-63746136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572128920	chr12:63746140-63746141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542807239	chr12:63746245-63746246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375729210	chr12:63746251-63746252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76460189	chr12:63746260-63746261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527487279	chr12:63746357-63746358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145469771	chr12:63746361-63746362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564990899	chr12:63746400-63746401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75900168	chr12:63746424-63746425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190105055	chr12:63746450-63746451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1520722	chr12:63746454-63746455	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569191250	chr12:63746484-63746485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531562310	chr12:63746519-63746520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551764698	chr12:63746523-63746524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114306731	chr12:63746548-63746549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571357979	chr12:63746588-63746589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534132077	chr12:63746617-63746618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75519501	chr12:63746669-63746670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547868835	chr12:63746678-63746679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79644777	chr12:63746680-63746681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369287866	chr12:63746707-63746708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181751009	chr12:63746712-63746713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571960948	chr12:63746759-63746760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140220865	chr12:63746881-63746882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186306934	chr12:63746884-63746885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145350447	chr12:63746903-63746904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs146441750	chr12:63746920-63746921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116512700	chr12:63746922-63746923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567752515	chr12:63746933-63746934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534712929	chr12:63746943-63746944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541119100	chr12:63747007-63747008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560952470	chr12:63747014-63747015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190427775	chr12:63747023-63747024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140900574	chr12:63747049-63747050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563212967	chr12:63747109-63747110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143146484	chr12:63747142-63747143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180839808	chr12:63747154-63747155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551319856	chr12:63747165-63747166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571294575	chr12:63747173-63747174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185439573	chr12:63747267-63747268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371359843	chr12:63747268-63747269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12809962	chr12:63747279-63747280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs190940681	chr12:63747286-63747287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71086662	chr12:63747310-63747311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374773581	chr12:63747314-63747315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368208199	chr12:63747316-63747317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375851877	chr12:63747318-63747319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77521470	chr12:63747320-63747321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201483640	chr12:63747322-63747323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	16620391	CNVD
Autism	21865298	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63743200-63747600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:63745400-63749000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:63745600-63747600	Weak transcription	Fetal Intestine Small	intestine
4	chr12:63745800-63747600	Weak transcription	HMEC	breast
5	chr12:63747400-63747800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr12:63747400-63749400	Enhancers	Fetal Kidney	kidney
7	chr12:63747600-63747800	Enhancers	Fetal Intestine Small	intestine
8	chr12:63747600-63748000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:63747600-63748000	Enhancers	HMEC	breast
10	chr12:63747800-63748600	Weak transcription	Fetal Intestine Small	intestine
11	chr12:63748600-63749600	Enhancers	Fetal Intestine Small	intestine
12	chr12:63749000-63749400	Enhancers	Fetal Intestine Large	intestine
13	chr12:63749000-63753600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:63753600-63755800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:63754000-63754400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr12:63754400-63754800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr12:63754400-63755400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:63755400-63755600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:63759400-63759800	Enhancers	Dnd41	blood
20	chr12:63775400-63778000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:63778000-63778200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr12:63778200-63779000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:63778200-63783200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr12:63779000-63781200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:63780600-63780800	Enhancers	Gastric	stomach
26	chr12:63780800-63781800	Weak transcription	Gastric	stomach
27	chr12:63781200-63782000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:63781200-63782200	Enhancers	Fetal Intestine Large	intestine
29	chr12:63781400-63782200	Enhancers	Fetal Intestine Small	intestine
30	chr12:63781600-63782000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:63781800-63782000	Enhancers	Gastric	stomach
32	chr12:63781800-63784400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:63782000-63782400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:63782000-63787600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:63782400-63784400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:63783200-63785000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:63783400-63784000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:63783600-63784600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr12:63783600-63784800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr12:63783800-63784400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr12:63783800-63784400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:63783800-63784400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr12:63784000-63784600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr12:63784600-63785200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr12:63785000-63785800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:63785200-63785400	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr12:63785800-63786400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr12:63787200-63787800	Enhancers	Fetal Kidney	kidney
49	chr12:63787200-63788600	Enhancers	Stomach Mucosa	stomach
50	chr12:63787600-63788000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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