Variant report

Variant	rs3774750
Chromosome Location	chr3:50208406-50208407
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:50207958-50208621	IMR90	lung:	n/a	n/a
2	FOS	chr3:50208198-50208488	MCF10A-Er-Src	breast:	n/a	chr3:50208329-50208340 chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
3	MXI1	chr3:50207579-50208710	IMR90	lung:	n/a	n/a
4	MXI1	chr3:50208119-50208479	Hela-S3	cervix:	n/a	n/a
5	FOXP2	chr3:50208125-50208509	PFSK-1	brain:	n/a	n/a
6	MAX	chr3:50208116-50208598	K562	blood:	n/a	chr3:50208330-50208339
7	FOS	chr3:50207950-50208586	HUVEC	blood vessel:	n/a	chr3:50208329-50208340 chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
8	NR3C1	chr3:50208133-50208491	A549	lung:	n/a	n/a
9	NR3C1	chr3:50208157-50208539	A549	lung:	n/a	n/a
10	ZEB1	chr3:50208098-50209914	HepG2	liver:	n/a	chr3:50209188-50209199 chr3:50209187-50209199 chr3:50209198-50209210
11	JUND	chr3:50208189-50208431	HepG2	liver:	n/a	chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208329-50208340 chr3:50208332-50208339
12	JUND	chr3:50208155-50208489	K562	blood:	n/a	chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208329-50208340 chr3:50208332-50208339
13	GABPA	chr3:50208059-50208508	Hela-S3	cervix:	n/a	n/a
14	MAZ	chr3:50207264-50208705	IMR90	lung:	n/a	chr3:50208330-50208339
15	USF1	chr3:50208201-50208438	HepG2	liver:	n/a	chr3:50208333-50208344
16	MAX	chr3:50208117-50208538	HUVEC	blood vessel:	n/a	chr3:50208330-50208339
17	ELK4	chr3:50208113-50208550	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr3:50207808-50208611	Hela-S3	cervix:	n/a	n/a
19	USF1	chr3:50208206-50208476	K562	blood:	n/a	chr3:50208333-50208344
20	JUN	chr3:50208124-50208550	HUVEC	blood vessel:	n/a	chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
21	POLR2A	chr3:50208182-50208590	Hela-S3	cervix:	n/a	n/a
22	GABPA	chr3:50208027-50208557	K562	blood:	n/a	n/a
23	MYC	chr3:50208106-50208514	HUVEC	blood vessel:	n/a	chr3:50208330-50208339
24	TAF1	chr3:50208089-50208507	Hela-S3	cervix:	n/a	n/a
25	MAFK	chr3:50208264-50208464	IMR90	lung:	n/a	chr3:50208329-50208339
26	USF1	chr3:50208205-50208463	SK-N-SH_RA	brain:	n/a	chr3:50208333-50208344
27	FOSL2	chr3:50208155-50208568	A549	lung:	n/a	chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
28	SMC3	chr3:50207918-50208486	Hela-S3	cervix:	n/a	chr3:50208064-50208072 chr3:50208401-50208409
29	MAX	chr3:50208252-50208502	K562	blood:	n/a	chr3:50208330-50208339
30	FOSL2	chr3:50208004-50208547	SK-N-SH	brain:	n/a	chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
31	JUND	chr3:50208267-50208524	HepG2	liver:	n/a	chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208329-50208340 chr3:50208332-50208339
32	GABPA	chr3:50208107-50208415	A549	lung:	n/a	n/a
33	CREB1	chr3:50208136-50208488	A549	lung:	n/a	n/a
34	FOS	chr3:50208179-50208455	MCF10A-Er-Src	breast:	n/a	chr3:50208329-50208340 chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
35	MAX	chr3:50208184-50208669	SK-N-SH	brain:	n/a	chr3:50208330-50208339
36	MAX	chr3:50208326-50208538	HepG2	liver:	n/a	chr3:50208330-50208339
37	MAX	chr3:50208191-50208503	NB4	blood:	n/a	chr3:50208330-50208339
38	ZBTB7A	chr3:50208141-50208410	K562	blood:	n/a	n/a
39	FOS	chr3:50208185-50208497	MCF10A-Er-Src	breast:	n/a	chr3:50208329-50208340 chr3:50208331-50208339 chr3:50208331-50208339 chr3:50208332-50208339
40	CHD2	chr3:50208148-50208510	HepG2	liver:	n/a	chr3:50208227-50208237
41	MYC	chr3:50208242-50208408	K562	blood:	n/a	chr3:50208330-50208339
42	E2F6	chr3:50208227-50208520	K562	blood:	n/a	n/a
43	BHLHE40	chr3:50208271-50208453	K562	blood:	n/a	n/a
44	MAX	chr3:50208049-50208528	Hela-S3	cervix:	n/a	chr3:50208330-50208339
45	POLR2A	chr3:50208355-50208429	Gliobla	brain:	n/a	n/a
46	GATA2	chr3:50208017-50208517	HUVEC	blood vessel:	n/a	n/a
47	USF1	chr3:50208194-50208496	K562	blood:	n/a	chr3:50208333-50208344
48	RAD21	chr3:50208282-50208479	IMR90	lung:	n/a	n/a
49	ZBTB7A	chr3:50208361-50208539	HepG2	liver:	n/a	n/a
50	USF2	chr3:50207980-50208511	Hela-S3	cervix:	n/a	chr3:50208334-50208345

No.	Distal block	Cell Line	Cell type
1	chr3:50194586..50199661-chr3:50206741..50210376,5	K562	blood:
2	chr3:50164983..50167115-chr3:50208238..50210374,2	MCF-7	breast:
3	chr3:50191401..50200098-chr3:50206213..50213809,14	MCF-7	breast:
4	chr3:50208138..50210089-chr3:50211604..50213556,2	MCF-7	breast:

Variant related genes	Relation type
SEMA3F	TF binding region
MIR566	TF binding region
ENSG00000001617	Chromatin interaction
ENSG00000235016	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11711407	0.86[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11714286	0.86[ASN][1000 genomes]
rs11714799	0.90[ASN][1000 genomes]
rs11717349	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13085567	0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1858828	0.82[JPT][hapmap]
rs2073726	0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2236942	0.81[CHB][hapmap]
rs2282749	0.86[CHB][hapmap]
rs2526383	0.85[ASN][1000 genomes]
rs34877766	0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs3755831	0.88[ASN][1000 genomes]
rs3774745	0.96[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3774749	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3774751	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67627084	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9858059	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834690	chr3:50101835-50267584	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers 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	24 gene(s)	inside rSNPs	diseases
2	nsv515986	chr3:50104307-50267584	Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Flanking Active TSS 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	24 gene(s)	inside rSNPs	diseases
3	nsv432418	chr3:50114496-50224196	Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	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
5	nsv876768	chr3:50144951-50267584	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs3774750	RBM6	cis	Esophagus Muscularis	GTEx
rs3774750	RBM6	Cis_1M	lymphoblastoid	RTeQTL
rs3774750	RBM6	cis	Heart Left Ventricle	GTEx
rs3774750	RBM6	cis	Whole Blood	GTEx
rs3774750	RBM6	cis	Nerve Tibial	GTEx
rs3774750	RBM6	cis	lung	GTEx
rs3774750	RBM6	cis	Thyroid	GTEx
rs3774750	RBM6	cis	Artery Aorta	GTEx
rs3774750	RBM6	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50194200-50208800	Weak transcription	Pancreas	Pancrea
2	chr3:50195400-50210200	Genic enhancers	Fetal Stomach	stomach
3	chr3:50195400-50210600	Enhancers	Left Ventricle	heart
4	chr3:50195400-50210800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:50196200-50211600	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr3:50197200-50211600	Genic enhancers	Esophagus	oesophagus
7	chr3:50199200-50209400	Enhancers	Placenta	Placenta
8	chr3:50200000-50209600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:50200000-50210400	Enhancers	Fetal Brain Male	brain
10	chr3:50200600-50211800	Enhancers	Right Ventricle	heart
11	chr3:50202000-50210600	Enhancers	A549	lung
12	chr3:50202200-50210400	Enhancers	Lung	lung
13	chr3:50202400-50208800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:50202800-50211000	Enhancers	Fetal Muscle Leg	muscle
15	chr3:50203000-50210000	Enhancers	Duodenum Mucosa	Duodenum
16	chr3:50203400-50211400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr3:50203800-50210000	Genic enhancers	HMEC	breast
18	chr3:50204000-50208800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:50204400-50211000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr3:50204600-50209600	Enhancers	HUVEC	blood vessel
21	chr3:50204600-50226600	Weak transcription	Brain Anterior Caudate	brain
22	chr3:50204800-50208600	Weak transcription	Psoas Muscle	Psoas
23	chr3:50204800-50210400	Enhancers	Stomach Smooth Muscle	stomach
24	chr3:50204800-50210600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr3:50204800-50211200	Weak transcription	Aorta	Aorta
26	chr3:50204800-50211800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr3:50205000-50208600	Enhancers	HepG2	liver
28	chr3:50205000-50209200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:50205000-50212800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:50205200-50208800	Flanking Active TSS	Hela-S3	cervix
31	chr3:50205400-50209200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr3:50205400-50210200	Genic enhancers	NHEK	skin
33	chr3:50205400-50211800	Enhancers	Stomach Mucosa	stomach
34	chr3:50205400-50226600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr3:50205400-50226600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr3:50205600-50208600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr3:50205600-50211200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr3:50205600-50211400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr3:50205800-50208800	Enhancers	Right Atrium	heart
40	chr3:50205800-50211800	Weak transcription	Fetal Kidney	kidney
41	chr3:50206200-50208600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr3:50206400-50208600	Genic enhancers	Gastric	stomach
43	chr3:50206400-50226600	Weak transcription	NHLF	lung
44	chr3:50206600-50209000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr3:50206600-50211200	Weak transcription	Ovary	ovary
46	chr3:50206600-50211600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr3:50207000-50208800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr3:50207000-50209200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr3:50207200-50208800	Enhancers	Osteobl	bone
50	chr3:50207200-50209000	Weak transcription	Small Intestine	intestine

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