Variant report

Variant	rs1624009
Chromosome Location	chr6:106740272-106740273
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:106738772..106740659-chr6:106743750..106745285,2	K562	blood:

Extended variants
information (count: 112 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10484575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11754416	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11756379	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11756420	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11759048	1.00[CEU][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.82[JPT][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11760170	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11961415	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1623780	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1624701	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1626224	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1626503	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1627312	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17488854	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17513225	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1766192	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1766196	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1766199	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1766200	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1766205	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1769962	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769963	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1769964	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769968	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1769970	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769971	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769972	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769974	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769975	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1769978	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1769981	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1832408	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2743560	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743561	0.83[YRI][hapmap]
rs2743562	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743563	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2743564	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2757132	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2757133	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2763210	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763211	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763212	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763214	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2763215	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763216	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763217	0.96[ASN][1000 genomes]
rs2763218	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2763221	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787521	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787525	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787527	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787528	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787529	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2787530	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787531	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787535	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787536	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787538	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787539	0.96[ASN][1000 genomes]
rs2787540	0.87[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787543	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787544	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787545	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2787546	0.96[ASN][1000 genomes]
rs2787547	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787549	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787551	0.96[ASN][1000 genomes]
rs2787552	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2787553	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2791114	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2791116	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2853338	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2853340	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3827647	0.96[ASN][1000 genomes]
rs41292420	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4310087	0.96[ASN][1000 genomes]
rs4607457	0.89[ASN][1000 genomes]
rs543465	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs577707	0.96[ASN][1000 genomes]
rs595875	0.96[ASN][1000 genomes]
rs626664	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs676099	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs687709	0.96[ASN][1000 genomes]
rs6920944	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6930834	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73520690	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522606	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522607	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522610	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522612	0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73522614	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522619	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522625	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73522642	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73522648	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs796707	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.89[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs960323	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932155	chr6:106281728-107030467	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1025900	chr6:106529777-106898421	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1018270	chr6:106531658-106908606	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv538399	chr6:106531658-106908606	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv1035110	chr6:106557281-106802212	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv538400	chr6:106557281-106802212	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv1022855	chr6:106570926-106802072	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv538401	chr6:106570926-106802072	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv532047	chr6:106591482-107143252	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
10	nsv1025963	chr6:106593639-106848778	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
11	nsv1020047	chr6:106597828-106912047	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv970664	chr6:106635267-106887670	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
13	nsv1030367	chr6:106667748-106802072	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers 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	21 gene(s)	inside rSNPs	diseases
14	nsv538403	chr6:106667748-106802072	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
15	nsv870375	chr6:106696090-107047892	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106695800-106740800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:106699200-106767400	Weak transcription	Stomach Mucosa	stomach
3	chr6:106711600-106762800	Weak transcription	Pancreas	Pancrea
4	chr6:106711600-106762800	Weak transcription	Right Ventricle	heart
5	chr6:106713600-106747800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:106717400-106741800	Weak transcription	Colonic Mucosa	Colon
7	chr6:106718000-106771600	Weak transcription	Fetal Brain Female	brain
8	chr6:106720600-106760400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:106723000-106771800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr6:106727400-106742000	Weak transcription	Brain Anterior Caudate	brain
11	chr6:106727400-106762200	Weak transcription	Ovary	ovary
12	chr6:106727600-106760800	Weak transcription	Brain Hippocampus Middle	brain
13	chr6:106731600-106745600	Weak transcription	Fetal Intestine Small	intestine
14	chr6:106734800-106762800	Weak transcription	Gastric	stomach
15	chr6:106734800-106771800	Weak transcription	Esophagus	oesophagus
16	chr6:106735200-106773000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:106735400-106742400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr6:106737000-106741400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr6:106738200-106740400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:106738200-106740600	Strong transcription	Fetal Intestine Large	intestine
21	chr6:106738200-106741200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:106738200-106741400	Strong transcription	Placenta	Placenta
23	chr6:106738200-106761400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr6:106738400-106740400	Strong transcription	Primary T cells from cord blood	blood
25	chr6:106738400-106740400	ZNF genes & repeats	HMEC	breast
26	chr6:106738400-106740400	Strong transcription	Osteobl	bone
27	chr6:106738400-106740600	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr6:106738400-106740800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr6:106738400-106741000	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:106738400-106741000	Strong transcription	Primary B cells from peripheral blood	blood
31	chr6:106738400-106741000	Strong transcription	Liver	Liver
32	chr6:106738400-106741000	Strong transcription	Fetal Thymus	thymus
33	chr6:106738600-106740400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:106738600-106740400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
35	chr6:106738600-106741000	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr6:106738600-106741000	Strong transcription	Duodenum Mucosa	Duodenum
37	chr6:106738600-106741400	Strong transcription	HSMM	muscle
38	chr6:106738600-106741800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:106738800-106740400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:106738800-106740400	ZNF genes & repeats	GM12878-XiMat	blood
41	chr6:106738800-106740800	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr6:106738800-106741000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr6:106738800-106741000	Strong transcription	Fetal Lung	lung
44	chr6:106739000-106740400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr6:106739000-106740600	Strong transcription	NH-A	brain
46	chr6:106739000-106741000	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr6:106739000-106741200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:106739000-106741400	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr6:106739200-106740400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:106739200-106740400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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