Variant report

Variant	rs35742476
Chromosome Location	chr19:18541785-18541786
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18538913-18542153	SK-N-MC	brain:	n/a	n/a
2	POLR2A	chr19:18538551-18551124	K562	blood:	n/a	n/a
3	POLR2A	chr19:18534926-18553479	K562	blood:	n/a	n/a
4	POLR2A	chr19:18541518-18542030	K562	blood:	n/a	n/a
5	POLR2A	chr19:18541346-18541806	HUVEC	blood vessel:	n/a	n/a
6	POLR2A	chr19:18541774-18542063	GM12878	blood:	n/a	n/a
7	POLR2A	chr19:18539622-18542014	K562	blood:	n/a	n/a
8	POLR2A	chr19:18541779-18542007	Hela-S3	cervix:	n/a	n/a
9	ZEB1	chr19:18541454-18541948	GM12878	blood:	n/a	chr19:18541737-18541746

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18495232..18499014-chr19:18539147..18542857,5	K562	blood:
2	chr19:18540459..18542781-chr19:18632920..18634658,2	K562	blood:
3	chr19:18527431..18533703-chr19:18536573..18544512,11	MCF-7	breast:
4	chr19:18539549..18542308-chr19:18573841..18576282,3	K562	blood:
5	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
6	chr19:18385251..18388025-chr19:18541664..18544540,2	K562	blood:

No data

Variant related genes	Relation type
SSBP4	TF binding region
ENSG00000105656	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000264175	Chromatin interaction

Extended variants
information (count: 88 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10164323	0.85[JPT][hapmap]
rs10402322	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10409346	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10409408	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10410797	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10413922	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10416993	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10418331	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10418554	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10420384	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10423802	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10426768	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1045631	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11086110	0.88[CEU][hapmap];0.88[CHB][hapmap];0.90[EUR][1000 genomes]
rs11668704	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11670392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11672385	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11879757	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12980726	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12982295	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12983263	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13344313	0.83[CHD][hapmap]
rs1469412	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1469413	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1971093	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2013069	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2162797	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2303692	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28534973	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2891676	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34213500	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.93[JPT][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35004712	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4006662	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4303657	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4580317	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4808135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4808802	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808803	0.94[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808805	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808806	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808807	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4808808	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4808811	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4808812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4808813	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55715336	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57923655	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6512268	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6512269	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6512270	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6512271	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7246788	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7247540	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7249760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7251640	1.00[CHB][hapmap]
rs7252130	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7252185	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7255936	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7256530	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7258891	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7259135	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7507218	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8100343	0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8102717	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8104247	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8106068	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8106332	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8111397	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8111582	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8111824	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.93[JPT][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8112372	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8112859	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs888668	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs888669	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
3	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
7	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
8	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
9	nsv911277	chr19:18520231-18552139	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
11	nsv911278	chr19:18526536-18550276	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
12	nsv911279	chr19:18533642-18550276	Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
13	nsv911280	chr19:18533642-18552139	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs35742476	SSBP4	cis	lymphoblastoid	seeQTL
rs35742476	LOC646044///SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs35742476	CYP4F11	cis	parietal	SCAN
rs35742476	ABHD8	cis	parietal	SCAN
rs35742476	ZNF93	cis	cerebellum	SCAN
rs35742476	ISYNA1	cis	parietal	SCAN
rs35742476	CHERP	cis	cerebellum	SCAN
rs35742476	SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs35742476	ZNF14	cis	parietal	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18531400-18543000	Enhancers	Fetal Brain Male	brain
2	chr19:18532800-18547600	Weak transcription	HepG2	liver
3	chr19:18536600-18542200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr19:18537400-18543800	Weak transcription	NHEK	skin
5	chr19:18537400-18544000	Weak transcription	HMEC	breast
6	chr19:18538000-18547600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr19:18538000-18548400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr19:18539200-18544000	Enhancers	Fetal Heart	heart
9	chr19:18540200-18543600	Weak transcription	Brain Angular Gyrus	brain
10	chr19:18540400-18542000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
11	chr19:18540400-18542600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr19:18540600-18541800	Enhancers	Primary B cells from cord blood	blood
13	chr19:18540600-18541800	Enhancers	Primary B cells from peripheral blood	blood
14	chr19:18540600-18541800	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr19:18540600-18541800	Genic enhancers	Fetal Intestine Small	intestine
16	chr19:18540600-18542400	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr19:18540600-18543400	Genic enhancers	Fetal Muscle Trunk	muscle
18	chr19:18540600-18543600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr19:18540600-18543600	Weak transcription	Esophagus	oesophagus
20	chr19:18540600-18543600	Weak transcription	Left Ventricle	heart
21	chr19:18540600-18543800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr19:18540600-18543800	Genic enhancers	Fetal Muscle Leg	muscle
23	chr19:18540600-18543800	Genic enhancers	Fetal Stomach	stomach
24	chr19:18540800-18541800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr19:18540800-18541800	Enhancers	Brain Germinal Matrix	brain
26	chr19:18540800-18542000	Enhancers	Primary T cells from cord blood	blood
27	chr19:18540800-18542000	Enhancers	Primary hematopoietic stem cells	blood
28	chr19:18540800-18542000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr19:18540800-18542200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr19:18540800-18542400	Weak transcription	Ovary	ovary
31	chr19:18540800-18542600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr19:18540800-18543000	Weak transcription	Right Atrium	heart
33	chr19:18540800-18543000	Weak transcription	Right Ventricle	heart
34	chr19:18540800-18543400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr19:18540800-18543600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr19:18540800-18543600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr19:18540800-18543600	Weak transcription	Adipose Nuclei	Adipose
38	chr19:18540800-18543600	Weak transcription	Colon Smooth Muscle	Colon
39	chr19:18540800-18543800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr19:18540800-18543800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr19:18540800-18543800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr19:18540800-18543800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:18540800-18543800	Weak transcription	Osteobl	bone
44	chr19:18540800-18544000	Weak transcription	Gastric	stomach
45	chr19:18540800-18544000	Weak transcription	Small Intestine	intestine
46	chr19:18540800-18545400	Weak transcription	A549	lung
47	chr19:18541000-18541800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr19:18541000-18541800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr19:18541000-18541800	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr19:18541000-18541800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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