Variant report

Variant	esv1844915
Chromosome Location	chr3:139648874-139654211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:488)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 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	chr3:139654108-139654260	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr3:139654009-139654199	K562	blood:	n/a	n/a
3	CEBPB	chr3:139653423-139653643	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr3:139653445-139653754	H1-hESC	embryonic stem cell:	n/a	n/a
5	CREB1	chr3:139653164-139654436	H1-hESC	embryonic stem cell:	n/a	chr3:139653971-139653984
6	CREB1	chr3:139653808-139654178	A549	lung:	n/a	chr3:139653971-139653984
7	CREB1	chr3:139653000-139654183	H1-hESC	embryonic stem cell:	n/a	chr3:139653971-139653984
8	CTBP2	chr3:139653274-139655142	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr3:139654100-139654250	HMF	breast:	n/a	n/a
10	CTCF	chr3:139653400-139653710	GM12878	blood:	n/a	n/a
11	CTCF	chr3:139653518-139653626	K562	blood:	n/a	n/a
12	CTCF	chr3:139653480-139653630	HEK293	kidney:	n/a	n/a
13	CTCF	chr3:139653980-139654130	GM12871	blood:	n/a	n/a
14	CTCF	chr3:139653499-139653609	HepG2	liver:	n/a	n/a
15	CTCF	chr3:139653500-139653650	AG09319	gingival:	n/a	n/a
16	CTCF	chr3:139653480-139653630	GM12871	blood:	n/a	n/a
17	CTCF	chr3:139653480-139653630	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr3:139653456-139653642	Fibrobl	skin:	n/a	n/a
19	CTCF	chr3:139653500-139653650	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr3:139654100-139654250	GM12865	blood:	n/a	n/a
21	CTCF	chr3:139653467-139653612	LNCaP	prostate:	n/a	n/a
22	CTCF	chr3:139653540-139653690	GM12875	blood:	n/a	n/a
23	CTCF	chr3:139653460-139653610	Caco-2	colon:	n/a	n/a
24	CTCF	chr3:139654128-139654228	GM12891	blood:	n/a	n/a
25	CTCF	chr3:139653517-139653565	GM19239	blood:	n/a	n/a
26	CTCF	chr3:139653432-139653666	ProgFib	skin:	n/a	n/a
27	CTCF	chr3:139654060-139654210	GM12875	blood:	n/a	n/a
28	CTCF	chr3:139653460-139653610	HPF	lung:	n/a	n/a
29	CTCF	chr3:139654080-139654230	NHEK	skin:	n/a	n/a
30	CTCF	chr3:139653467-139653629	GM12878	blood:	n/a	n/a
31	CTCF	chr3:139653453-139653649	GM19238	blood:	n/a	n/a
32	CTCF	chr3:139652720-139652870	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:139653500-139653650	HRE	kidney:	n/a	n/a
34	CTCF	chr3:139653160-139653310	GM12867	blood:	n/a	n/a
35	CTCF	chr3:139653400-139653712	MCF-7	breast:	n/a	n/a
36	CTCF	chr3:139653513-139653600	GM10248	blood:	n/a	n/a
37	CTCF	chr3:139653500-139653650	NHLF	lung:	n/a	n/a
38	CTCF	chr3:139654087-139654336	NHEK	skin:	n/a	n/a
39	CTCF	chr3:139654093-139654205	ProgFib	skin:	n/a	n/a
40	CTCF	chr3:139653370-139653718	T-47D	breast:	n/a	n/a
41	CTCF	chr3:139653480-139653630	SAEC	small airway:	n/a	n/a
42	CTCF	chr3:139653460-139653610	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr3:139653377-139653656	HepG2	liver:	n/a	n/a
44	CTCF	chr3:139653220-139654254	A549	lung:	n/a	n/a
45	CTCF	chr3:139652822-139652867	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:139653397-139653844	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:139654100-139654250	GM12875	blood:	n/a	n/a
48	CTCF	chr3:139653460-139653610	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr3:139653412-139653687	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:139653453-139653667	A549	lung:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:139653545-139653595	GM12892	blood:	n/a
2	chr3:139653872-139653922	NB4	blood:	n/a
3	chr3:139653928-139653978	HL-60	blood:	n/a
4	chr3:139649460-139649510	ovcar-3	ovarian:	n/a
5	chr3:139653573-139653623	NHDF-neo	bronchial:	n/a
6	chr3:139653915-139653965	BE2_C	brain:	n/a
7	chr3:139653915-139653965	AG09319	gingival:	n/a
8	chr3:139653573-139653623	SK-N-MC	brain:	n/a
9	chr3:139653915-139653965	AG10803	skin:	n/a
10	chr3:139653431-139653481	AG04450	lung:	fetal
11	chr3:139653915-139653965	HEK293	kidney:	embryo
12	chr3:139653431-139653481	HL-60	blood:	n/a
13	chr3:139653573-139653623	A549	lung:	n/a
14	chr3:139653928-139653978	PANC-1	pancreas:	n/a
15	chr3:139653928-139653978	GM12878	blood:	n/a
16	chr3:139653928-139653978	Caco-2	colon:	n/a
17	chr3:139653431-139653481	SK-N-SH_RA	brain:	n/a
18	chr3:139653915-139653965	NHBE	bronchial:	n/a
19	chr3:139649460-139649510	HUVEC	blood vessel:	n/a
20	chr3:139649460-139649510	LNCaP	prostate:	n/a
21	chr3:139653928-139653978	HAEpiC	amniotic membrane:	n/a
22	chr3:139653431-139653481	BE2_C	brain:	n/a
23	chr3:139653573-139653623	RPTEC	kidney:	n/a
24	chr3:139653915-139653965	SK-N-SH_RA	brain:	n/a
25	chr3:139649460-139649510	Jurkat	blood:	n/a
26	chr3:139653915-139653965	HCT-116	colon:	n/a
27	chr3:139653573-139653623	HAEpiC	amniotic membrane:	n/a
28	chr3:139653431-139653481	Hela-S3	cervix:	n/a
29	chr3:139653328-139653378	LNCaP	prostate:	n/a
30	chr3:139653928-139653978	HCF	heart:	n/a
31	chr3:139653328-139653378	T-47D	breast:	n/a
32	chr3:139653431-139653481	HCM	heart:	n/a
33	chr3:139653915-139653965	A549	lung:	n/a
34	chr3:139653573-139653623	MCF-7	breast:	n/a
35	chr3:139653928-139653978	HRPEpiC	eye:	n/a
36	chr3:139653431-139653481	GM19239	blood:	n/a
37	chr3:139653328-139653378	MCF-7	breast:	n/a
38	chr3:139649460-139649510	HRE	kidney:	n/a
39	chr3:139653545-139653595	GM19239	blood:	n/a
40	chr3:139653431-139653481	ovcar-3	ovarian:	n/a
41	chr3:139653872-139653922	GM06990	blood:	n/a
42	chr3:139653573-139653623	NB4	blood:	n/a
43	chr3:139653328-139653378	H1-hESC	embryonic stem cell:	embryo
44	chr3:139653872-139653922	SKMC	muscle:	n/a
45	chr3:139653872-139653922	HRCEpiC	kidney:	n/a
46	chr3:139653915-139653965	AG09309	skin:	n/a
47	chr3:139653928-139653978	LNCaP	prostate:	n/a
48	chr3:139653915-139653965	SK-N-SH	brain:	n/a
49	chr3:139653928-139653978	HRCEpiC	kidney:	n/a
50	chr3:139653928-139653978	BJ	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:139282929..139283874-chr3:139652757..139653752,4	MCF-7	breast:
2	chr3:139645968..139647481-chr3:139648116..139649820,2	MCF-7	breast:
3	chr3:139438799..139439673-chr3:139652877..139653733,2	MCF-7	breast:
4	chr3:139641405..139642937-chr3:139647406..139649250,2	K562	blood:
5	chr3:139307203..139308238-chr3:139653078..139653999,6	MCF-7	breast:
6	chr3:139347937..139348556-chr3:139653424..139653964,2	MCF-7	breast:
7	chr3:139270922..139271855-chr3:139653137..139653973,3	MCF-7	breast:
8	chr3:139646808..139649286-chr3:139653164..139655013,2	MCF-7	breast:
9	chr3:139437070..139437910-chr3:139653098..139654016,8	MCF-7	breast:

No data

Variant related genes	Relation type
CLSTN2	TF binding region
CLSTN2	CpG island
ENSG00000158258	chromatin interactions

Extended variants
information (count: 203 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:203 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9869519	chr3:139648874-139648875	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557150527	chr3:139648875-139648876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs9850110	chr3:139648953-139648954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs56370145	chr3:139648965-139648966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553431345	chr3:139648981-139648982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78588480	chr3:139648996-139648997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542209030	chr3:139649011-139649012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9850149	chr3:139649029-139649030	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530839816	chr3:139649038-139649039	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544501700	chr3:139649051-139649052	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs183484216	chr3:139649067-139649068	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533146984	chr3:139649090-139649091	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546417819	chr3:139649096-139649097	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs189365354	chr3:139649101-139649102	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs531344143	chr3:139649127-139649128	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181221681	chr3:139649138-139649139	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544845821	chr3:139649167-139649168	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530592018	chr3:139649196-139649197	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568480114	chr3:139649206-139649207	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs116373441	chr3:139649221-139649222	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550843025	chr3:139649236-139649237	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570759083	chr3:139649240-139649241	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs533564325	chr3:139649242-139649243	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540031759	chr3:139649253-139649254	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553242423	chr3:139649257-139649258	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs573305775	chr3:139649258-139649259	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs13085522	chr3:139649297-139649298	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs58306556	chr3:139649326-139649327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75857069	chr3:139649327-139649328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555832344	chr3:139649335-139649336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs398062853	chr3:139649339-139649340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374880046	chr3:139649340-139649341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575687754	chr3:139649365-139649366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544562988	chr3:139649372-139649373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35562869	chr3:139649377-139649378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564362224	chr3:139649385-139649386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139858598	chr3:139649405-139649406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142722318	chr3:139649460-139649461	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs560061176	chr3:139649468-139649469	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs528999645	chr3:139649522-139649523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116009821	chr3:139649584-139649585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs13063473	chr3:139649589-139649590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546434202	chr3:139649614-139649615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114535393	chr3:139649649-139649650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1895858	chr3:139649663-139649664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs537898005	chr3:139649718-139649719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539715092	chr3:139649795-139649796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547184877	chr3:139649845-139649846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558022817	chr3:139649869-139649870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571484946	chr3:139649870-139649871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139642800-139651600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:139647600-139649200	Enhancers	Ovary	ovary
3	chr3:139648000-139649600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr3:139648800-139649600	Enhancers	HMEC	breast
5	chr3:139649600-139653400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr3:139651400-139651800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr3:139651600-139651800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:139651600-139651800	Enhancers	Spleen	Spleen
9	chr3:139651800-139653200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:139651800-139653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:139652400-139652600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
12	chr3:139652400-139652600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
13	chr3:139652600-139652800	Enhancers	Brain Hippocampus Middle	brain
14	chr3:139653200-139653400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:139653200-139653400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr3:139653200-139653400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
17	chr3:139653200-139653400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:139653200-139653400	Bivalent Enhancer	Adipose Nuclei	Adipose
19	chr3:139653200-139653400	Enhancers	Brain Angular Gyrus	brain
20	chr3:139653200-139653400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr3:139653200-139653400	Enhancers	Ovary	ovary
22	chr3:139653200-139653400	Enhancers	Pancreas	Pancrea
23	chr3:139653200-139653400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr3:139653200-139653400	Flanking Bivalent TSS/Enh	HSMMtube	muscle
25	chr3:139653200-139653600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr3:139653200-139653600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr3:139653200-139653600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:139653200-139653600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:139653200-139653600	Bivalent Enhancer	Fetal Intestine Small	intestine
30	chr3:139653200-139653600	Bivalent Enhancer	Placenta	Placenta
31	chr3:139653200-139654000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:139653200-139654200	Enhancers	Fetal Brain Male	brain
33	chr3:139653200-139654800	Active TSS	Brain Anterior Caudate	brain
34	chr3:139653200-139655000	Active TSS	Brain Cingulate Gyrus	brain
35	chr3:139653200-139655200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr3:139653200-139655200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
37	chr3:139653200-139655200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
38	chr3:139653200-139655400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr3:139653200-139655600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr3:139653200-139655600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
41	chr3:139653200-139656000	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr3:139653400-139653600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:139653400-139653600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr3:139653400-139653600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr3:139653400-139653600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
46	chr3:139653400-139653600	Bivalent Enhancer	Fetal Intestine Large	intestine
47	chr3:139653400-139653600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr3:139653400-139653600	Flanking Active TSS	Ovary	ovary
49	chr3:139653400-139653600	Active TSS	Psoas Muscle	Psoas
50	chr3:139653400-139653600	Enhancers	Right Atrium	heart

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