Variant report

Variant	rs11763027
Chromosome Location	chr7:5790239-5790240
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:5790126..5791962-chr7:5819797..5822715,2	MCF-7	breast:
2	chr7:5778904..5781083-chr7:5790150..5792640,2	MCF-7	breast:
3	chr7:5790125..5792090-chr7:5812066..5813881,3	K562	blood:

Variant related genes	Relation type
ENSG00000011275	Chromatin interaction

Extended variants
information (count: 143 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs10225845	0.83[AMR][1000 genomes]
rs10271741	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs10807950	1.00[ASN][1000 genomes]
rs10951961	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1640231	0.83[ASN][1000 genomes]
rs1640234	1.00[JPT][hapmap]
rs1725186	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1725187	0.94[ASN][1000 genomes]
rs1990835	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2008418	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2008425	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2112008	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2112010	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2161012	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2161016	0.83[AMR][1000 genomes]
rs2161017	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2345663	0.84[AFR][1000 genomes]
rs2345665	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2345863	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2345864	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2693951	0.83[AMR][1000 genomes]
rs2881234	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs28874635	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2908430	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3735288	0.94[ASN][1000 genomes]
rs3857756	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs3943984	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4720636	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4720639	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4720643	1.00[CHB][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4720645	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4720648	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4724714	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4724716	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4724720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4724721	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4724723	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4724727	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4724732	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs4724734	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60912551	0.88[AFR][1000 genomes]
rs62455878	0.87[ASN][1000 genomes]
rs6463508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6463509	0.83[ASN][1000 genomes]
rs6463511	0.89[EUR][1000 genomes]
rs6463512	0.84[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs6463515	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66467570	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6944453	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6945676	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6947405	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6953412	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6956990	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6957150	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6969486	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6974576	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs710939	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs710940	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs710942	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73343309	0.82[AFR][1000 genomes]
rs73343338	0.83[AFR][1000 genomes]
rs7784394	1.00[ASN][1000 genomes]
rs7790499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792177	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7794571	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7809914	0.87[ASN][1000 genomes]
rs852261	1.00[ASN][1000 genomes]
rs852262	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852264	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852378	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852381	0.83[AMR][1000 genomes]
rs852383	0.83[AMR][1000 genomes]
rs852393	1.00[ASN][1000 genomes]
rs852395	1.00[ASN][1000 genomes]
rs852398	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852399	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852401	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852403	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs852404	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852405	1.00[ASN][1000 genomes]
rs852407	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852408	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852411	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs852412	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852413	1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs852414	1.00[ASN][1000 genomes]
rs852416	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852418	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852419	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs852437	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852438	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852439	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852440	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852442	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs852443	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852449	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852451	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852455	0.94[ASN][1000 genomes]
rs852458	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852459	0.94[ASN][1000 genomes]
rs852460	0.94[ASN][1000 genomes]
rs852462	0.94[ASN][1000 genomes]
rs852465	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852466	0.94[ASN][1000 genomes]
rs852467	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	0.94[ASN][1000 genomes]
rs852476	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852477	0.94[ASN][1000 genomes]
rs852480	0.83[AMR][1000 genomes]
rs852487	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852490	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs852514	0.94[ASN][1000 genomes]
rs852515	0.83[ASN][1000 genomes]
rs852518	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852521	0.94[ASN][1000 genomes]
rs852523	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852524	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs852525	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs941016	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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	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
8	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
9	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
10	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
11	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
12	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
13	nsv830891	chr7:5726301-5895460	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
14	nsv1028601	chr7:5748982-5919098	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
15	nsv1034215	chr7:5748982-6056619	Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
16	nsv1016690	chr7:5749222-6056619	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
17	nsv1027679	chr7:5760731-6056619	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
18	nsv464293	chr7:5778796-5891221	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv464294	chr7:5778796-5891221	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	nsv605987	chr7:5778796-5891221	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
21	esv2764038	chr7:5785999-5893967	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5753200-5794400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:5762000-5820400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:5765200-5790400	Weak transcription	Psoas Muscle	Psoas
4	chr7:5768800-5798200	Weak transcription	Colonic Mucosa	Colon
5	chr7:5774200-5800600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:5781200-5790600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:5781200-5792400	Weak transcription	Gastric	stomach
8	chr7:5781400-5790400	Weak transcription	Right Ventricle	heart
9	chr7:5781400-5790600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr7:5781400-5799600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:5781400-5816800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:5781800-5790600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr7:5782800-5794400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr7:5783600-5798200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:5783800-5790400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr7:5784000-5819600	Weak transcription	Fetal Heart	heart
17	chr7:5784200-5792800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:5784200-5792800	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr7:5784200-5798000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr7:5784400-5792800	Strong transcription	Primary T cells from cord blood	blood
21	chr7:5784800-5792800	Strong transcription	Dnd41	blood
22	chr7:5785000-5792800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:5785000-5795400	Strong transcription	Fetal Muscle Trunk	muscle
24	chr7:5785200-5807000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:5785400-5793000	Strong transcription	Primary B cells from peripheral blood	blood
26	chr7:5785600-5792600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr7:5785600-5794200	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr7:5785800-5793000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:5786000-5791200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:5786000-5792800	Strong transcription	K562	blood
31	chr7:5786000-5798000	Weak transcription	Fetal Brain Male	brain
32	chr7:5786200-5790600	Weak transcription	Fetal Intestine Small	intestine
33	chr7:5786200-5791600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:5786200-5795000	Weak transcription	HUVEC	blood vessel
35	chr7:5786400-5790400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr7:5786400-5792400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:5786600-5790400	Weak transcription	Brain Germinal Matrix	brain
38	chr7:5787200-5792200	Weak transcription	Fetal Kidney	kidney
39	chr7:5787600-5794000	Weak transcription	Stomach Mucosa	stomach
40	chr7:5787800-5794600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:5788000-5790400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:5788000-5791600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr7:5788200-5792600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr7:5788600-5792800	Strong transcription	Osteobl	bone
45	chr7:5789000-5792600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr7:5789000-5792800	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr7:5789000-5794200	Strong transcription	Fetal Thymus	thymus
48	chr7:5789200-5790800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:5789200-5792800	Strong transcription	HSMM	muscle
50	chr7:5789200-5793000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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