Variant report

Variant	esv3394751
Chromosome Location	chr3:112928562-112932960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:1038)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:112930587-112930930	H1-hESC	embryonic stem cell:	n/a	chr3:112930861-112930875
2	BACH1	chr3:112931290-112931581	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:112929513-112929539	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr3:112929519-112929712	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:112929490-112929663	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr3:112929519-112929521	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr3:112929934-112930238	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr3:112931173-112931260	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD1	chr3:112930818-112930958	H1-hESC	embryonic stem cell:	n/a	chr3:112930937-112930947
10	CHD2	chr3:112929356-112929657	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr3:112929701-112931583	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr3:112930639-112930851	MCF-7	breast:	n/a	n/a
13	CTCF	chr3:112932820-112932970	AG10803	skin:	n/a	n/a
14	CTCF	chr3:112930961-112930984	ProgFib	skin:	n/a	n/a
15	CTCF	chr3:112930880-112931030	GM12866	blood:	n/a	n/a
16	CTCF	chr3:112930878-112931034	LNCaP	prostate:	n/a	n/a
17	CTCF	chr3:112930600-112930750	HFF	foreskin:	n/a	n/a
18	CTCF	chr3:112930938-112930991	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr3:112930602-112930609	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:112930800-112930950	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr3:112932800-112932950	AG09319	gingival:	n/a	n/a
22	CTCF	chr3:112930820-112930970	AG09319	gingival:	n/a	n/a
23	CTCF	chr3:112930820-112930970	AG04449	skin:	n/a	n/a
24	CTCF	chr3:112930820-112930970	HepG2	liver:	n/a	n/a
25	CTCF	chr3:112930860-112931010	AG04450	lung:	n/a	n/a
26	CTCF	chr3:112930890-112931043	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:112930840-112930990	NHEK	skin:	n/a	n/a
28	CTCF	chr3:112930597-112930601	MCF-7	breast:	n/a	n/a
29	CTCF	chr3:112930900-112931050	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr3:112932860-112933010	AG04449	skin:	n/a	n/a
31	CTCF	chr3:112932816-112932961	NHEK	skin:	n/a	n/a
32	CTCF	chr3:112930880-112931030	GM12871	blood:	n/a	n/a
33	CTCF	chr3:112932852-112932864	Fibrobl	skin:	n/a	n/a
34	CTCF	chr3:112930840-112930990	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr3:112930860-112931010	HAc	cerebellar:	n/a	n/a
36	CTCF	chr3:112930820-112930970	SAEC	small airway:	n/a	n/a
37	CTCF	chr3:112930840-112930990	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr3:112931540-112931690	NHEK	skin:	n/a	n/a
39	CTCF	chr3:112930840-112930990	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr3:112930860-112931010	GM12868	blood:	n/a	n/a
41	CTCF	chr3:112930733-112930831	NHEK	skin:	n/a	n/a
42	CTCF	chr3:112930780-112930930	AG04449	skin:	n/a	n/a
43	CTCF	chr3:112930600-112930750	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr3:112930931-112931015	Fibrobl	skin:	n/a	n/a
45	CTCF	chr3:112930860-112931010	HCM	heart:	n/a	n/a
46	CTCF	chr3:112930918-112931029	LNCaP	prostate:	n/a	n/a
47	CTCF	chr3:112930840-112930990	Caco-2	colon:	n/a	n/a
48	CTCF	chr3:112930880-112931030	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:112930803-112931052	IMR90	lung:	n/a	n/a
50	CTCF	chr3:112930932-112931014	MCF-7	breast:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112931202-112931252	BE2_C	brain:	n/a
2	chr3:112931202-112931252	BE2_C	brain:	n/a
3	chr3:112931194-112931244	GM19239	blood:	n/a
4	chr3:112931202-112931252	HUVEC	blood vessel:	n/a
5	chr3:112931202-112931252	AG10803	skin:	n/a
6	chr3:112931126-112931176	NHDF-neo	bronchial:	n/a
7	chr3:112930675-112930725	K562	blood:	n/a
8	chr3:112930438-112930488	HRE	kidney:	n/a
9	chr3:112930077-112930127	HUVEC	blood vessel:	n/a
10	chr3:112931348-112931398	HRCEpiC	kidney:	n/a
11	chr3:112931348-112931398	HIPEpiC	eye:	n/a
12	chr3:112929672-112929722	GM12878	blood:	n/a
13	chr3:112930187-112930237	HepG2	liver:	n/a
14	chr3:112931182-112931232	AG09309	skin:	n/a
15	chr3:112931354-112931404	BJ	skin:	n/a
16	chr3:112931126-112931176	AoSMC	blood vessel:	n/a
17	chr3:112930187-112930237	HPAEpiC	pulmonary alveolar:	n/a
18	chr3:112930438-112930488	SK-N-SH	brain:	n/a
19	chr3:112929830-112929880	HEEpiC	esophagus:	n/a
20	chr3:112930782-112930832	HUVEC	blood vessel:	n/a
21	chr3:112931182-112931232	NT2-D1	testis:	n/a
22	chr3:112930675-112930725	AG04450	lung:	fetal
23	chr3:112930187-112930237	CMK	blood:	n/a
24	chr3:112931202-112931252	CMK	blood:	n/a
25	chr3:112932345-112932395	HCPEpiC	choroid plexus:	n/a
26	chr3:112931496-112931546	HNPCEpiC	eye:	n/a
27	chr3:112929830-112929880	SAEC	small airway:	n/a
28	chr3:112930438-112930488	HAEpiC	amniotic membrane:	n/a
29	chr3:112931354-112931404	NHDF-neo	bronchial:	n/a
30	chr3:112929835-112929885	GM12892	blood:	n/a
31	chr3:112930782-112930832	IMR90	lung:	fetal
32	chr3:112930438-112930488	HRPEpiC	eye:	n/a
33	chr3:112931202-112931252	Hepatocyte	liver:	n/a
34	chr3:112929835-112929885	HCF	heart:	n/a
35	chr3:112931354-112931404	SKMC	muscle:	n/a
36	chr3:112932345-112932395	GM06990	blood:	n/a
37	chr3:112932345-112932395	ovcar-3	ovarian:	n/a
38	chr3:112931126-112931176	ECC-1	luminal epithelium:	n/a
39	chr3:112931496-112931546	SK-N-SH	brain:	n/a
40	chr3:112931182-112931232	PrEC	prostate:	n/a
41	chr3:112930675-112930725	ovcar-3	ovarian:	n/a
42	chr3:112931496-112931546	Caco-2	colon:	n/a
43	chr3:112930187-112930237	GM06990	blood:	n/a
44	chr3:112930077-112930127	PFSK-1	brain:	n/a
45	chr3:112931126-112931176	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:112929672-112929722	SK-N-MC	brain:	n/a
47	chr3:112930782-112930832	ProgFib	skin:	n/a
48	chr3:112931182-112931232	GM12878	blood:	n/a
49	chr3:112930782-112930832	ovcar-3	ovarian:	n/a
50	chr3:112931202-112931252	ProgFib	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:61735022..61735793-chr3:112930479..112931247,2	HCT-116	colon:
2	chr3:112929722..112932026-chr3:112933958..112936481,2	K562	blood:
3	chr3:112929165..112932026-chr3:112933299..112935458,2	K562	blood:
4	chr3:112875811..112877981-chr3:112929321..112930900,2	MCF-7	breast:

No data

Variant related genes	Relation type
BOC	TF binding region
BOC	CpG island
ENSG00000269089	chromatin interactions
ENSG00000144857	chromatin interactions
ENSG00000167996	chromatin interactions
ENSG00000240057	chromatin interactions

Extended variants
information (count: 171 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:171 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138768215	chr3:112928619-112928620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557221314	chr3:112928620-112928621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368620735	chr3:112928632-112928633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12635028	chr3:112928656-112928657	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs576777348	chr3:112928690-112928691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76342564	chr3:112928695-112928696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7639036	chr3:112928762-112928763	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs551087880	chr3:112928782-112928783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540296038	chr3:112928796-112928797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565245122	chr3:112928848-112928849	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs148963338	chr3:112928856-112928857	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs550940586	chr3:112928859-112928860	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569523271	chr3:112928880-112928881	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs528753256	chr3:112928885-112928886	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548976199	chr3:112928888-112928889	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs79535837	chr3:112928913-112928914	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs547321105	chr3:112929014-112929015	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs143119201	chr3:112929016-112929017	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs73235124	chr3:112929032-112929033	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs142885762	chr3:112929035-112929036	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs10934227	chr3:112929036-112929037	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs200402094	chr3:112929058-112929059	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs200128512	chr3:112929072-112929073	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs7641396	chr3:112929075-112929076	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555674291	chr3:112929076-112929077	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200989756	chr3:112929079-112929080	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139082119	chr3:112929087-112929088	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138761748	chr3:112929091-112929092	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs537775891	chr3:112929107-112929108	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs575475495	chr3:112929159-112929160	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542485924	chr3:112929312-112929313	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs11715505	chr3:112929334-112929335	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376163572	chr3:112929359-112929360	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs77045306	chr3:112929363-112929364	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs540236648	chr3:112929364-112929365	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs546050851	chr3:112929377-112929378	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs565375148	chr3:112929420-112929421	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs557692069	chr3:112929421-112929422	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs532538506	chr3:112929479-112929480	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs13070573	chr3:112929574-112929575	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4364141	chr3:112929617-112929618	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7641880	chr3:112929621-112929622	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113974038	chr3:112929669-112929670	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs7642061	chr3:112929748-112929749	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs567177808	chr3:112929749-112929750	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs528042747	chr3:112929762-112929763	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs546321861	chr3:112929814-112929815	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs76538338	chr3:112929831-112929832	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs538384613	chr3:112929833-112929834	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs67668649	chr3:112929836-112929837	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

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
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Breast cancer	17142309	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ductal carcinoma	22052326	CNVD

Chromatin state (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112919400-112929200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:112922600-112929200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr3:112923600-112929200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:112926400-112929200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:112926600-112928800	Weak transcription	Fetal Muscle Trunk	muscle
6	chr3:112927200-112929200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:112927200-112929200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:112927200-112929200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:112928000-112929000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:112928200-112928600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:112928200-112929200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:112928200-112929200	Enhancers	Colon Smooth Muscle	Colon
13	chr3:112928200-112929200	Enhancers	Fetal Muscle Leg	muscle
14	chr3:112928400-112929000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr3:112928400-112929200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr3:112928400-112929200	Enhancers	Fetal Stomach	stomach
17	chr3:112928400-112929200	Enhancers	Rectal Smooth Muscle	rectum
18	chr3:112928400-112929400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr3:112928600-112929000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr3:112928800-112929000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:112928800-112929000	Active TSS	Stomach Smooth Muscle	stomach
22	chr3:112928800-112929200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:112928800-112929200	Enhancers	Fetal Muscle Trunk	muscle
24	chr3:112928800-112929400	Enhancers	Fetal Lung	lung
25	chr3:112929000-112929200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr3:112929000-112929200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr3:112929000-112929200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:112929000-112929200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:112929000-112929200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr3:112929000-112929200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:112929000-112929200	Enhancers	Fetal Brain Female	brain
32	chr3:112929000-112929400	Enhancers	Fetal Brain Male	brain
33	chr3:112929000-112929600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr3:112929000-112929600	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr3:112929000-112929800	Enhancers	Pancreas	Pancrea
36	chr3:112929000-112930000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr3:112929200-112929400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
38	chr3:112929200-112929400	Enhancers	H9 Cell Line	embryonic stem cell
39	chr3:112929200-112929400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:112929200-112929400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr3:112929200-112929400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:112929200-112929400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:112929200-112929400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:112929200-112929400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr3:112929200-112929400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr3:112929200-112929400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
47	chr3:112929200-112929400	Enhancers	Esophagus	oesophagus
48	chr3:112929200-112929400	Bivalent Enhancer	Fetal Intestine Large	intestine
49	chr3:112929200-112929400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
50	chr3:112929200-112929400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle

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