Variant report

Variant	rs58648044
Chromosome Location	chr3:50248954-50248955
allele	G/T
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	HNF4G	chr3:50248615-50248972	HepG2	liver:	n/a	chr3:50248767-50248782 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248767-50248781 chr3:50248767-50248782 chr3:50248768-50248781 chr3:50248773-50248781 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248765-50248780 chr3:50248774-50248782
2	ZNF143	chr3:50248812-50249068	K562	blood:	n/a	n/a
3	RCOR1	chr3:50248845-50249005	K562	blood:	n/a	n/a
4	EP300	chr3:50248515-50249021	HepG2	liver:	n/a	n/a
5	HDAC2	chr3:50248515-50248987	HepG2	liver:	n/a	chr3:50248773-50248781
6	ZEB1	chr3:50247773-50249085	HepG2	liver:	n/a	n/a
7	CEBPB	chr3:50248633-50248969	HepG2	liver:	n/a	chr3:50248817-50248834
8	HEY1	chr3:50247085-50248970	HepG2	liver:	n/a	n/a
9	ZEB1	chr3:50247640-50249020	HepG2	liver:	n/a	n/a
10	HNF4A	chr3:50247719-50248995	HepG2	liver:	n/a	chr3:50248767-50248782 chr3:50247964-50247979 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248767-50248781 chr3:50247987-50248002 chr3:50248767-50248782 chr3:50248768-50248781 chr3:50248773-50248781 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248774-50248782
11	HNF4G	chr3:50248586-50248973	HepG2	liver:	n/a	chr3:50248767-50248782 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248767-50248781 chr3:50248767-50248782 chr3:50248768-50248781 chr3:50248773-50248781 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248765-50248780 chr3:50248774-50248782
12	ZNF384	chr3:50248808-50249078	K562	blood:	n/a	n/a
13	POLR2A	chr3:50247154-50249010	HepG2	liver:	n/a	n/a
14	MYBL2	chr3:50247690-50249028	HepG2	liver:	n/a	n/a
15	FOXA1	chr3:50247738-50248970	HepG2	liver:	n/a	n/a
16	YY1	chr3:50247948-50248969	HepG2	liver:	n/a	chr3:50248737-50248748
17	POLR2A	chr3:50247042-50248992	HepG2	liver:	n/a	n/a
18	SP1	chr3:50247710-50249016	HepG2	liver:	n/a	chr3:50248739-50248753 chr3:50248746-50248760
19	HEY1	chr3:50247113-50248969	HepG2	liver:	n/a	n/a
20	POLR2A	chr3:50248696-50248967	HepG2	liver:	n/a	n/a
21	HNF4A	chr3:50248542-50248972	HepG2	liver:	n/a	chr3:50248767-50248782 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248767-50248781 chr3:50248767-50248782 chr3:50248768-50248781 chr3:50248773-50248781 chr3:50248768-50248780 chr3:50248767-50248782 chr3:50248774-50248782
22	POLR2A	chr3:50248732-50248961	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:50241794..50243896-chr3:50246798..50250002,3	MCF-7	breast:

Variant related genes	Relation type
SLC38A3	TF binding region
ENSG00000188338	Chromatin interaction

Extended variants
information (count: 121 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs1046956	0.85[EUR][1000 genomes]
rs11130248	0.85[ASN][1000 genomes]
rs11919418	0.86[EUR][1000 genomes]
rs12054403	0.85[ASN][1000 genomes]
rs12485390	0.96[ASN][1000 genomes]
rs12485909	0.92[ASN][1000 genomes]
rs12487392	0.90[ASN][1000 genomes]
rs12488235	0.86[ASN][1000 genomes]
rs12488302	0.87[ASN][1000 genomes]
rs12492683	0.85[ASN][1000 genomes]
rs12492880	0.87[ASN][1000 genomes]
rs12493693	0.87[ASN][1000 genomes]
rs12494414	0.82[ASN][1000 genomes]
rs12495261	0.85[ASN][1000 genomes]
rs12496815	0.81[ASN][1000 genomes]
rs12497018	0.88[ASN][1000 genomes]
rs12498048	0.99[ASN][1000 genomes]
rs12632110	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12637671	0.84[EUR][1000 genomes]
rs12721544	0.88[ASN][1000 genomes]
rs13059311	0.83[EUR][1000 genomes]
rs13064381	0.87[EUR][1000 genomes]
rs13067082	0.86[EUR][1000 genomes]
rs14321	0.85[EUR][1000 genomes]
rs2006199	0.90[ASN][1000 genomes]
rs2071203	0.88[ASN][1000 genomes]
rs2071204	0.87[ASN][1000 genomes]
rs2071205	0.87[ASN][1000 genomes]
rs2071801	0.83[ASN][1000 genomes]
rs2073497	0.85[ASN][1000 genomes]
rs2073500	0.85[ASN][1000 genomes]
rs2229647	0.87[ASN][1000 genomes]
rs2233476	0.84[ASN][1000 genomes]
rs2236940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2236941	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2236943	0.98[ASN][1000 genomes]
rs2236944	0.97[ASN][1000 genomes]
rs2236946	0.85[ASN][1000 genomes]
rs2236949	0.80[ASN][1000 genomes]
rs2269430	0.85[ASN][1000 genomes]
rs2269432	0.87[ASN][1000 genomes]
rs2282750	1.00[ASN][1000 genomes]
rs2285043	0.87[ASN][1000 genomes]
rs2285044	0.87[ASN][1000 genomes]
rs2298953	0.98[ASN][1000 genomes]
rs2298954	0.98[ASN][1000 genomes]
rs2624833	0.82[EUR][1000 genomes]
rs2624835	0.81[EUR][1000 genomes]
rs2624838	0.87[EUR][1000 genomes]
rs2624841	0.82[EUR][1000 genomes]
rs3213621	0.83[ASN][1000 genomes]
rs35137368	0.93[EUR][1000 genomes]
rs35219849	0.94[EUR][1000 genomes]
rs35455589	0.85[ASN][1000 genomes]
rs35587949	0.85[ASN][1000 genomes]
rs3774739	0.81[ASN][1000 genomes]
rs3774748	0.81[ASN][1000 genomes]
rs3774752	0.83[ASN][1000 genomes]
rs3774753	0.87[ASN][1000 genomes]
rs3774754	0.83[ASN][1000 genomes]
rs3774755	0.84[ASN][1000 genomes]
rs4141407	1.00[ASN][1000 genomes]
rs4688679	0.84[ASN][1000 genomes]
rs4688682	0.97[ASN][1000 genomes]
rs4688683	0.92[ASN][1000 genomes]
rs4688724	0.84[ASN][1000 genomes]
rs4688725	0.83[ASN][1000 genomes]
rs4688728	0.83[ASN][1000 genomes]
rs4688732	0.85[ASN][1000 genomes]
rs4688733	0.85[ASN][1000 genomes]
rs4688734	0.87[ASN][1000 genomes]
rs4688736	0.85[ASN][1000 genomes]
rs4688738	0.85[ASN][1000 genomes]
rs4688741	0.98[ASN][1000 genomes]
rs4688742	0.98[ASN][1000 genomes]
rs4688744	1.00[ASN][1000 genomes]
rs4688746	0.87[ASN][1000 genomes]
rs57944420	0.83[ASN][1000 genomes]
rs57978992	0.88[ASN][1000 genomes]
rs58181992	0.85[ASN][1000 genomes]
rs60276643	0.89[ASN][1000 genomes]
rs6807194	0.93[EUR][1000 genomes]
rs72932959	0.87[ASN][1000 genomes]
rs72932987	0.85[ASN][1000 genomes]
rs7645537	0.98[ASN][1000 genomes]
rs9311449	0.83[ASN][1000 genomes]
rs9830408	0.96[ASN][1000 genomes]
rs9852677	0.85[ASN][1000 genomes]
rs9858297	0.85[EUR][1000 genomes]
rs9882618	0.89[ASN][1000 genomes]
rs9883222	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs58648044	RBM6	Cis_1M	lymphoblastoid	RTeQTL
rs58648044	HYAL3	cis	Esophagus Muscularis	GTEx

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50244000-50251200	Enhancers	Pancreas	Pancrea
2	chr3:50244000-50254600	Weak transcription	Esophagus	oesophagus
3	chr3:50244000-50263800	Weak transcription	Right Atrium	heart
4	chr3:50244200-50263800	Weak transcription	Left Ventricle	heart
5	chr3:50244400-50249600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:50244400-50263800	Weak transcription	Right Ventricle	heart
7	chr3:50246400-50249200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:50246400-50249400	Weak transcription	Brain Angular Gyrus	brain
9	chr3:50246400-50249600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:50246600-50249400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr3:50246600-50249400	Weak transcription	Brain Substantia Nigra	brain
12	chr3:50246600-50250600	Weak transcription	Fetal Muscle Leg	muscle
13	chr3:50246800-50251400	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr3:50247200-50249200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr3:50247400-50249200	Weak transcription	Adipose Nuclei	Adipose
16	chr3:50247400-50250000	Enhancers	Fetal Intestine Small	intestine
17	chr3:50247400-50250200	Enhancers	Fetal Intestine Large	intestine
18	chr3:50247400-50250400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:50247400-50264400	Weak transcription	Ovary	ovary
20	chr3:50247600-50249000	Enhancers	Small Intestine	intestine
21	chr3:50247600-50249400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr3:50247600-50250600	Weak transcription	Fetal Brain Female	brain
23	chr3:50247800-50249000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:50247800-50249400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:50247800-50249400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:50248000-50249200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr3:50248000-50249600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:50248000-50250000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr3:50248000-50250400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr3:50248200-50250600	Enhancers	Psoas Muscle	Psoas
31	chr3:50248200-50253000	Enhancers	Brain Hippocampus Middle	brain
32	chr3:50248400-50255200	Weak transcription	Spleen	Spleen
33	chr3:50248600-50249600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr3:50248600-50249600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr3:50248800-50249000	Flanking Active TSS	Liver	Liver
36	chr3:50248800-50249200	Weak transcription	Brain Anterior Caudate	brain
37	chr3:50248800-50249400	Enhancers	HepG2	liver
38	chr3:50248800-50249600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr3:50248800-50249600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:50248800-50249600	Weak transcription	Stomach Mucosa	stomach
41	chr3:50248800-50250000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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