Variant report

Variant	rs61737738
Chromosome Location	chr3:50311476-50311477
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr3:50311458-50312426	HCT-116	colon:	n/a	n/a
2	ESRRA	chr3:50311461-50312181	GM12878	blood:	n/a	n/a
3	EGR1	chr3:50311437-50312305	HCT-116	colon:	n/a	chr3:50311864-50311878
4	CTCF	chr3:50311286-50313009	SK-N-SH	brain:	n/a	n/a
5	POLR2A	chr3:50311256-50312035	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr3:50305532-50313853	HepG2	liver:	n/a	n/a
7	CTCF	chr3:50311342-50312406	A549	lung:	n/a	n/a
8	CTCF	chr3:50311440-50311590	GM12873	blood:	n/a	n/a
9	CTCF	chr3:50311380-50311530	HUVEC	blood vessel:	n/a	n/a
10	E2F6	chr3:50311385-50312229	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr3:50311440-50311590	GM12874	blood:	n/a	n/a
12	POLR2A	chr3:50311303-50313257	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr3:50311400-50311550	GM12873	blood:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50310426..50313247-chr3:50328333..50331056,2	K562	blood:
2	chr3:50311428..50312361-chr3:50358911..50359787,2	K562	blood:
3	chr3:50309059..50311667-chr3:50323698..50326427,2	K562	blood:
4	chr3:50310332..50311966-chr3:50374071..50376123,2	MCF-7	breast:
5	chr3:50310650..50313903-chr3:50314125..50318251,8	MCF-7	breast:
6	chr3:50262511..50266127-chr3:50309039..50312887,6	K562	blood:
7	chr3:50262511..50265125-chr3:50311115..50313229,2	K562	blood:
8	chr3:50311192..50313650-chr3:50358965..50360786,3	K562	blood:
9	chr3:50309725..50313756-chr3:50357883..50363910,8	K562	blood:
10	chr3:50305234..50312110-chr3:50326257..50332221,8	MCF-7	breast:
11	chr3:50310399..50313142-chr3:50335615..50338582,3	K562	blood:
12	chr3:50303839..50307896-chr3:50307992..50312285,6	K562	blood:
13	chr3:50296030..50318456-chr3:50318822..50339499,66	MCF-7	breast:
14	chr3:50307238..50313479-chr3:50353130..50365794,18	MCF-7	breast:
15	chr3:50304620..50307086-chr3:50310040..50312285,3	K562	blood:
16	chr3:50296610..50299539-chr3:50310066..50312117,3	K562	blood:
17	chr3:50300460..50314689-chr3:50349154..50363682,34	MCF-7	breast:
18	chr3:50271706..50275857-chr3:50303511..50313889,17	MCF-7	breast:

No data

Variant related genes	Relation type
LSMEM2	TF binding region
SEMA3B	TF binding region
ENSG00000230454	Chromatin interaction
ENSG00000214706	Chromatin interaction
ENSG00000068001	Chromatin interaction
ENSG00000114378	Chromatin interaction
ENSG00000243477	Chromatin interaction
ENSG00000114383	Chromatin interaction
ENSG00000179564	Chromatin interaction
ENSG00000068028	Chromatin interaction
ENSG00000232352	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000186792	Chromatin interaction
ENSG00000012171	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12490837	0.96[AFR][1000 genomes]
rs2229647	0.96[AFR][1000 genomes]
rs2233476	0.90[AFR][1000 genomes]
rs2233482	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2236946	0.82[AFR][1000 genomes]
rs35587949	0.87[AFR][1000 genomes]
rs4688679	0.90[AFR][1000 genomes]
rs4688728	0.87[AFR][1000 genomes]
rs4688736	0.96[AFR][1000 genomes]
rs58780990	1.00[AMR][1000 genomes]
rs59476380	0.84[AFR][1000 genomes]
rs59556423	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60983897	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61275090	1.00[AMR][1000 genomes]
rs61689858	1.00[AMR][1000 genomes]
rs72932956	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72932962	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72932964	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72932983	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72934803	1.00[AMR][1000 genomes]
rs72934806	1.00[AMR][1000 genomes]
rs72934814	1.00[AMR][1000 genomes]
rs72934815	1.00[AMR][1000 genomes]
rs72934824	1.00[AMR][1000 genomes]
rs72934827	1.00[AMR][1000 genomes]
rs72934830	1.00[AMR][1000 genomes]
rs928946	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
6	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
7	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
8	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
9	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
10	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
11	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
12	nsv523560	chr3:50172397-50339163	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
13	nsv460529	chr3:50178011-50324672	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
14	nsv460530	chr3:50178011-50324672	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
15	nsv590252	chr3:50178011-50324672	Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
16	nsv1002916	chr3:50187646-50311666	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
17	nsv536564	chr3:50187646-50311666	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv1014256	chr3:50187646-50339163	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
19	nsv536565	chr3:50187646-50339163	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
20	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
21	nsv590253	chr3:50196418-50337422	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
22	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
24	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
25	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
26	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
27	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
28	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
29	nsv590257	chr3:50302830-50393640	Genic enhancers Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
30	nsv590256	chr3:50302830-50420554	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
31	nsv876774	chr3:50302830-50436827	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
32	nsv876773	chr3:50302830-50480131	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
33	nsv834693	chr3:50302830-50507964	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50306800-50316000	Weak transcription	Aorta	Aorta
2	chr3:50308800-50316000	Weak transcription	HSMMtube	muscle
3	chr3:50310200-50313800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:50310200-50313800	Bivalent Enhancer	Fetal Thymus	thymus
5	chr3:50310400-50312000	Genic enhancers	HepG2	liver
6	chr3:50310400-50312200	Enhancers	A549	lung
7	chr3:50310400-50312200	Genic enhancers	Hela-S3	cervix
8	chr3:50310400-50312800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
9	chr3:50310400-50313800	Enhancers	Spleen	Spleen
10	chr3:50310600-50312200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:50310600-50314600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
12	chr3:50310800-50311600	Enhancers	Stomach Mucosa	stomach
13	chr3:50310800-50312600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
14	chr3:50310800-50312600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
15	chr3:50310800-50312800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
16	chr3:50310800-50313600	Bivalent Enhancer	Fetal Stomach	stomach
17	chr3:50310800-50314000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
18	chr3:50310800-50314200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
19	chr3:50310800-50314200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
20	chr3:50310800-50314400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr3:50310800-50325800	Weak transcription	HSMM	muscle
22	chr3:50311000-50311600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr3:50311000-50311600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr3:50311000-50311600	Active TSS	Brain Anterior Caudate	brain
25	chr3:50311000-50311600	Enhancers	Brain Cingulate Gyrus	brain
26	chr3:50311000-50311600	Enhancers	Brain Substantia Nigra	brain
27	chr3:50311000-50311800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
28	chr3:50311000-50311800	Enhancers	Esophagus	oesophagus
29	chr3:50311000-50311800	Enhancers	HMEC	breast
30	chr3:50311000-50311800	Enhancers	K562	blood
31	chr3:50311000-50312000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:50311000-50312000	Weak transcription	Left Ventricle	heart
33	chr3:50311000-50312000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
34	chr3:50311000-50312200	Enhancers	Adipose Nuclei	Adipose
35	chr3:50311000-50312200	Bivalent Enhancer	Fetal Intestine Large	intestine
36	chr3:50311000-50312200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr3:50311000-50312200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr3:50311000-50312400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
39	chr3:50311000-50312400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:50311000-50312600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:50311000-50312600	Bivalent Enhancer	Primary B cells from cord blood	blood
42	chr3:50311000-50312600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr3:50311000-50312600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:50311000-50312600	Weak transcription	Right Atrium	heart
45	chr3:50311000-50312600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
46	chr3:50311000-50312800	Genic enhancers	Fetal Intestine Small	intestine
47	chr3:50311000-50312800	Enhancers	Right Ventricle	heart
48	chr3:50311000-50313000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
49	chr3:50311000-50313200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
50	chr3:50311000-50313200	Bivalent Enhancer	HUVEC	blood vessel

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