Variant report

Variant	rs852404
Chromosome Location	chr7:5716805-5716806
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:5708885..5710643-chr7:5716339..5719013,2	K562	blood:
2	chr7:5634585..5636582-chr7:5716195..5717760,2	K562	blood:
3	chr7:5563906..5565672-chr7:5715265..5717638,2	K562	blood:
4	chr7:5567652..5570729-chr7:5716334..5720767,4	MCF-7	breast:
5	chr7:5603045..5605168-chr7:5716278..5719037,2	MCF-7	breast:
6	chr7:5561140..5562775-chr7:5716624..5718720,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000075624	Chromatin interaction
ENSG00000263900	Chromatin interaction

Extended variants
information (count: 140 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:124)

rs_ID	r²[population]
rs10225845	0.89[EUR][1000 genomes]
rs10271741	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10807950	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10951961	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11763027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1628786	1.00[AMR][1000 genomes]
rs1640231	0.83[ASN][1000 genomes]
rs1640234	1.00[JPT][hapmap]
rs1725186	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1725187	0.94[ASN][1000 genomes]
rs1990835	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2008418	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2008425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2112008	1.00[ASN][1000 genomes]
rs2161012	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2161017	0.83[AMR][1000 genomes]
rs2345665	0.83[AMR][1000 genomes]
rs2345863	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2345864	1.00[ASN][1000 genomes]
rs2693951	1.00[AMR][1000 genomes]
rs2881234	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28874635	0.87[ASN][1000 genomes]
rs2908430	0.94[ASN][1000 genomes]
rs3735288	0.94[ASN][1000 genomes]
rs3857756	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs3943984	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4720636	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4720639	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4720643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[ASN][1000 genomes]
rs4720645	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4724714	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4724716	1.00[ASN][1000 genomes]
rs4724720	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4724721	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4724723	1.00[ASN][1000 genomes]
rs4724727	1.00[CEU][hapmap];0.87[ASN][1000 genomes]
rs4724732	0.87[ASN][1000 genomes]
rs4724734	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs62455878	0.87[ASN][1000 genomes]
rs6463508	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6463509	0.83[ASN][1000 genomes]
rs6463512	0.83[ASN][1000 genomes]
rs6463515	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs66467570	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6944453	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6945676	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6947405	1.00[ASN][1000 genomes]
rs6953412	0.83[AMR][1000 genomes]
rs6956990	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6957150	0.83[AMR][1000 genomes]
rs6969486	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs710939	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs710940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs710942	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7784394	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7790499	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7792177	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7794571	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7803040	1.00[JPT][hapmap]
rs7809914	0.87[ASN][1000 genomes]
rs852260	0.83[AMR][1000 genomes]
rs852261	1.00[ASN][1000 genomes]
rs852262	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852264	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852377	0.83[AMR][1000 genomes]
rs852378	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852381	1.00[AMR][1000 genomes]
rs852383	1.00[AMR][1000 genomes]
rs852393	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852395	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852398	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852399	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852401	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852403	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852405	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852411	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs852412	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852413	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852414	1.00[ASN][1000 genomes]
rs852416	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852418	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852419	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs852437	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852438	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852439	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852440	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852442	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852443	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852449	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852451	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852455	0.94[ASN][1000 genomes]
rs852458	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852459	0.94[ASN][1000 genomes]
rs852460	1.00[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs852462	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852465	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852466	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852467	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852469	0.94[ASN][1000 genomes]
rs852471	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852474	1.00[ASN][1000 genomes]
rs852475	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852476	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852477	0.94[ASN][1000 genomes]
rs852480	1.00[AMR][1000 genomes]
rs852486	1.00[CEU][hapmap]
rs852487	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852490	1.00[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852495	1.00[AMR][1000 genomes]
rs852509	0.85[AMR][1000 genomes]
rs852514	0.94[ASN][1000 genomes]
rs852515	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs852518	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852521	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852523	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852524	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852525	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852536	1.00[AMR][1000 genomes]
rs852541	1.00[AMR][1000 genomes]
rs852543	1.00[AMR][1000 genomes]
rs852544	1.00[AMR][1000 genomes]
rs941016	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
2	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
3	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
4	nsv530983	chr7:5370746-6070852	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
5	nsv916391	chr7:5417945-5889565	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
6	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
7	nsv482449	chr7:5557585-5743673	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	294 gene(s)	inside rSNPs	diseases
8	nsv1033556	chr7:5565080-6186815	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
9	nsv538710	chr7:5565080-6186815	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
10	nsv530467	chr7:5617816-5815082	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
11	nsv1017612	chr7:5629728-5819144	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
12	nsv1021989	chr7:5629728-6186815	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
13	nsv887417	chr7:5667645-5760860	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
14	nsv887418	chr7:5675305-5772551	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
15	nsv887419	chr7:5703669-5820383	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
16	nsv1028652	chr7:5706207-5769489	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5674800-5728200	Weak transcription	Small Intestine	intestine
2	chr7:5691200-5721000	Weak transcription	Pancreas	Pancrea
3	chr7:5692600-5717400	Weak transcription	Hela-S3	cervix
4	chr7:5699200-5723000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:5702000-5717600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:5702000-5730600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:5702400-5717000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:5702400-5721400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr7:5702600-5717200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr7:5702600-5717200	Weak transcription	Aorta	Aorta
11	chr7:5702600-5717400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr7:5702600-5717600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:5702600-5718000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:5702800-5727200	Weak transcription	Psoas Muscle	Psoas
15	chr7:5707600-5717200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:5707600-5717200	Weak transcription	A549	lung
17	chr7:5707600-5717400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:5707600-5717600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:5707600-5719000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:5707600-5721000	Weak transcription	Stomach Mucosa	stomach
21	chr7:5707800-5718000	Weak transcription	K562	blood
22	chr7:5708400-5717200	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr7:5708800-5717600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:5709200-5717200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:5709200-5717200	Weak transcription	Fetal Intestine Large	intestine
26	chr7:5710600-5717600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:5710600-5718200	Weak transcription	Lung	lung
28	chr7:5710800-5717000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:5710800-5717400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr7:5710800-5717600	Weak transcription	Colonic Mucosa	Colon
31	chr7:5710800-5721200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr7:5711000-5717200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr7:5711400-5717600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:5711600-5717400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr7:5711600-5717400	Weak transcription	HSMMtube	muscle
36	chr7:5712200-5717200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:5712400-5717000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:5712400-5717400	Weak transcription	Primary B cells from cord blood	blood
39	chr7:5712600-5717000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr7:5712600-5717200	Weak transcription	Brain Hippocampus Middle	brain
41	chr7:5712600-5717200	Weak transcription	Brain Substantia Nigra	brain
42	chr7:5712600-5717200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr7:5712600-5717200	Weak transcription	NHDF-Ad	bronchial
44	chr7:5712600-5717400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr7:5712600-5717400	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr7:5712600-5719200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:5712800-5717400	Weak transcription	Brain Anterior Caudate	brain
48	chr7:5713000-5717000	Weak transcription	NHLF	lung
49	chr7:5713000-5717200	Weak transcription	Brain Angular Gyrus	brain
50	chr7:5713000-5730200	Weak transcription	Gastric	stomach

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