Variant report

Variant	nsv1010219
Chromosome Location	chr3:111856709-111923647
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:366)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:111886557-111887019	GM12878	blood:	n/a	n/a
2	ATF2	chr3:111886526-111887068	GM12878	blood:	n/a	n/a
3	BACH1	chr3:111919082-111919194	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:111862155-111862429	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:111886595-111886876	GM12878	blood:	n/a	chr3:111886782-111886791
6	BCL11A	chr3:111886588-111886970	GM12878	blood:	n/a	chr3:111886782-111886791
7	BHLHE40	chr3:111886625-111886908	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:111862307-111862410	GM12878	blood:	n/a	n/a
9	CEBPB	chr3:111896376-111896590	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr3:111860746-111860830	Hela-S3	cervix:	n/a	chr3:111860794-111860805
11	CEBPB	chr3:111860659-111860980	A549	lung:	n/a	chr3:111860794-111860805
12	CEBPB	chr3:111896244-111896553	IMR90	lung:	n/a	n/a
13	CEBPB	chr3:111860637-111860970	IMR90	lung:	n/a	chr3:111860794-111860805
14	CEBPB	chr3:111918586-111918855	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:111860615-111860982	HepG2	liver:	n/a	chr3:111860794-111860805
16	CEBPB	chr3:111860709-111860886	H1-hESC	embryonic stem cell:	n/a	chr3:111860794-111860805
17	CEBPB	chr3:111860661-111860905	K562	blood:	n/a	chr3:111860794-111860805
18	CHD2	chr3:111886701-111886898	GM12878	blood:	n/a	n/a
19	CTCF	chr3:111857520-111857670	SK-N-SH_RA	brain:	n/a	chr3:111857643-111857652
20	CTCF	chr3:111884695-111884865	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:111904780-111904930	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr3:111918500-111918650	SAEC	small airway:	n/a	n/a
23	CTCF	chr3:111860402-111860430	GM13976	blood:	n/a	n/a
24	CTCF	chr3:111918500-111918650	GM12865	blood:	n/a	n/a
25	CTCF	chr3:111904570-111904824	GM12892	blood:	n/a	n/a
26	CTCF	chr3:111904580-111904730	AG04449	skin:	n/a	n/a
27	CTCF	chr3:111912042-111912084	LNCaP	prostate:	n/a	n/a
28	CTCF	chr3:111884691-111884792	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:111918520-111918670	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr3:111896320-111896470	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr3:111896354-111896412	NHEK	skin:	n/a	n/a
32	CTCF	chr3:111904664-111904759	GM12891	blood:	n/a	n/a
33	CTCF	chr3:111904580-111904730	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr3:111918560-111918710	A549	lung:	n/a	n/a
35	CTCF	chr3:111904560-111904710	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr3:111868780-111868930	GM12866	blood:	n/a	n/a
37	CTCF	chr3:111918580-111918730	HAc	cerebellar:	n/a	n/a
38	CTCF	chr3:111904675-111904726	Medullo	brain:	n/a	n/a
39	CTCF	chr3:111918500-111918650	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr3:111904669-111904803	GM13977	blood:	n/a	n/a
41	CTCF	chr3:111902649-111902712	GM13976	blood:	n/a	n/a
42	CTCF	chr3:111918500-111918650	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr3:111896349-111896429	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr3:111904653-111904801	GM10266	blood:	n/a	n/a
45	CTCF	chr3:111918540-111918690	Caco-2	colon:	n/a	n/a
46	CTCF	chr3:111918460-111918610	HAc	cerebellar:	n/a	n/a
47	CTCF	chr3:111857580-111857730	HCPEpiC	choroid plexus:	n/a	chr3:111857643-111857652
48	CTCF	chr3:111918440-111918590	RPTEC	kidney:	n/a	n/a
49	CTCF	chr3:111864780-111864930	GM12871	blood:	n/a	n/a
50	CTCF	chr3:111902547-111902554	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:111903603-111903653	GM12878	blood:	n/a
2	chr3:111904806-111904856	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:111904892-111904942	HRPEpiC	eye:	n/a
4	chr3:111901903-111901953	CMK	blood:	n/a
5	chr3:111903603-111903653	T-47D	breast:	n/a
6	chr3:111903603-111903653	NHBE	bronchial:	n/a
7	chr3:111903603-111903653	PANC-1	pancreas:	n/a
8	chr3:111904806-111904856	HRE	kidney:	n/a
9	chr3:111904703-111904753	HRCEpiC	kidney:	n/a
10	chr3:111901903-111901953	AG04450	lung:	fetal
11	chr3:111916760-111916810	Caco-2	colon:	n/a
12	chr3:111901903-111901953	Jurkat	blood:	n/a
13	chr3:111904703-111904753	SK-N-MC	brain:	n/a
14	chr3:111904806-111904856	RPTEC	kidney:	n/a
15	chr3:111904892-111904942	SK-N-SH	brain:	n/a
16	chr3:111904703-111904753	NHDF-neo	bronchial:	n/a
17	chr3:111901903-111901953	RPTEC	kidney:	n/a
18	chr3:111901903-111901953	GM12892	blood:	n/a
19	chr3:111904703-111904753	HNPCEpiC	eye:	n/a
20	chr3:111904703-111904753	HUVEC	blood vessel:	n/a
21	chr3:111916760-111916810	HEK293	kidney:	embryo
22	chr3:111916760-111916810	Jurkat	blood:	n/a
23	chr3:111904703-111904753	SAEC	small airway:	n/a
24	chr3:111904703-111904753	U87	brain:	n/a
25	chr3:111903603-111903653	HRCEpiC	kidney:	n/a
26	chr3:111916760-111916810	MCF10A-Er-Src	breast:	n/a
27	chr3:111916760-111916810	PANC-1	pancreas:	n/a
28	chr3:111916760-111916810	AG10803	skin:	n/a
29	chr3:111904703-111904753	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:111904806-111904856	NHBE	bronchial:	n/a
31	chr3:111903603-111903653	MCF10A-Er-Src	breast:	n/a
32	chr3:111904806-111904856	ECC-1	luminal epithelium:	n/a
33	chr3:111904892-111904942	AoSMC	blood vessel:	n/a
34	chr3:111904892-111904942	K562	blood:	n/a
35	chr3:111901903-111901953	GM12891	blood:	n/a
36	chr3:111904892-111904942	GM06990	blood:	n/a
37	chr3:111916760-111916810	BJ	skin:	n/a
38	chr3:111904806-111904856	SK-N-SH_RA	brain:	n/a
39	chr3:111904892-111904942	HNPCEpiC	eye:	n/a
40	chr3:111904806-111904856	NT2-D1	testis:	n/a
41	chr3:111904806-111904856	GM06990	blood:	n/a
42	chr3:111916760-111916810	HRPEpiC	eye:	n/a
43	chr3:111916760-111916810	HCPEpiC	choroid plexus:	n/a
44	chr3:111916760-111916810	LNCaP	prostate:	n/a
45	chr3:111904806-111904856	SK-N-MC	brain:	n/a
46	chr3:111916760-111916810	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:111904806-111904856	NHDF-neo	bronchial:	n/a
48	chr3:111904703-111904753	Jurkat	blood:	n/a
49	chr3:111903603-111903653	Caco-2	colon:	n/a
50	chr3:111903603-111903653	BE2_C	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:111916552..111919160-chr3:111921905..111924645,2	K562	blood:
2	chr3:111858864..111861858-chr3:112359276..112360974,2	MCF-7	breast:
3	chr3:111851024..111853542-chr3:111855899..111858560,2	K562	blood:
4	chr3:111916552..111919160-chr3:111921905..111924645,2	K562	blood:
5	chr2:183179551..183180178-chr3:111918314..111918885,2	MCF-7	breast:
6	chr3:111856051..111856906-chr3:112237978..112238501,2	MCF-7	breast:
7	chr3:111859837..111862167-chr3:112256624..112258984,2	MCF-7	breast:

No data

Variant related genes	Relation type
GCSAM	TF binding region
ENSG00000244144	TF binding region
GCSAM	CpG island
ENSG00000244144	CpG island
ENSG00000091986	chromatin interactions
ENSG00000261488	chromatin interactions
ENSG00000144848	chromatin interactions
ENSG00000174500	chromatin interactions

Extended variants
information (count: 2264 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2264 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116122387	chr3:111856838-111856839	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs149770497	chr3:111856921-111856922	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs554502012	chr3:111856951-111856952	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs572506651	chr3:111856955-111856956	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs182092366	chr3:111856986-111856987	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs557619847	chr3:111857034-111857035	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs147877108	chr3:111857095-111857096	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs543021459	chr3:111857114-111857115	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs185339873	chr3:111857234-111857235	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116475421	chr3:111857299-111857300	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190995767	chr3:111857313-111857314	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561640034	chr3:111857358-111857359	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs530747772	chr3:111857375-111857376	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547597832	chr3:111857383-111857384	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183556109	chr3:111857392-111857393	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs576476556	chr3:111857523-111857524	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567777110	chr3:111857540-111857541	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs6803848	chr3:111857569-111857570	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565655890	chr3:111857580-111857581	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532832298	chr3:111857693-111857694	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs1994772	chr3:111857750-111857751	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs60567823	chr3:111857771-111857772	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs187442398	chr3:111857782-111857783	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111603677	chr3:111857796-111857797	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532335100	chr3:111857800-111857801	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141605044	chr3:111857804-111857805	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192968826	chr3:111857877-111857878	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs72256707	chr3:111857888-111857889	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs71970791	chr3:111857890-111857891	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537768826	chr3:111857961-111857962	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs534574852	chr3:111858001-111858002	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571070678	chr3:111858009-111858010	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112478776	chr3:111858039-111858040	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs11718471	chr3:111858117-111858118	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs183738789	chr3:111858197-111858198	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs61585647	chr3:111858317-111858318	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs398062689	chr3:111858321-111858322	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573298494	chr3:111858378-111858379	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs1032398	chr3:111858474-111858475	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs138797534	chr3:111858506-111858507	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575171643	chr3:111858561-111858562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544117576	chr3:111858570-111858571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563900982	chr3:111858575-111858576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148870876	chr3:111858588-111858589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540099720	chr3:111858614-111858615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77503762	chr3:111858618-111858619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529011107	chr3:111858649-111858650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548974420	chr3:111858661-111858662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562489757	chr3:111858683-111858684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371966872	chr3:111858697-111858698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111848200-111857000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:111848400-111856800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:111852200-111857000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr3:111852200-111857600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:111852200-111863400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:111852400-111857000	Enhancers	Primary B cells from cord blood	blood
7	chr3:111852400-111857200	Enhancers	Primary B cells from peripheral blood	blood
8	chr3:111852600-111857600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:111853200-111857000	Enhancers	Stomach Mucosa	stomach
10	chr3:111853400-111867400	Weak transcription	Gastric	stomach
11	chr3:111853600-111857000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr3:111853800-111857000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:111854200-111856800	Weak transcription	Fetal Intestine Small	intestine
14	chr3:111854200-111857000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr3:111854600-111857000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:111854600-111858000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:111854800-111857600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr3:111854800-111857800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr3:111855000-111857400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr3:111855000-111857600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:111855000-111858000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr3:111855200-111858000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:111855400-111856800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr3:111855400-111857000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr3:111855400-111857600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:111855400-111858000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:111855600-111857000	Enhancers	Primary hematopoietic stem cells	blood
28	chr3:111855800-111857000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:111855800-111857000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr3:111855800-111857200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr3:111855800-111857200	Enhancers	Duodenum Mucosa	Duodenum
32	chr3:111856200-111857800	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr3:111856200-111860200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr3:111856200-111867400	Weak transcription	Thymus	Thymus
35	chr3:111856200-111867600	Weak transcription	Left Ventricle	heart
36	chr3:111856400-111857800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr3:111856400-111861800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr3:111856400-111862400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr3:111856600-111857000	Enhancers	Brain Cingulate Gyrus	brain
40	chr3:111856600-111857600	Enhancers	GM12878-XiMat	blood
41	chr3:111856800-111857200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:111856800-111857400	Enhancers	Fetal Intestine Small	intestine
43	chr3:111857000-111857200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr3:111857000-111858400	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr3:111857000-111861000	Weak transcription	Primary hematopoietic stem cells	blood
46	chr3:111857200-111860200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:111858400-111858800	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr3:111858800-111862400	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr3:111860200-111860400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:111860200-111860600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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