Variant report

Variant	rs62394550
Chromosome Location	chr6:26034252-26034253
allele	C/G
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	TEAD4	chr6:26030925-26034594	K562	blood:	n/a	n/a
2	MYC	chr6:26033700-26034352	MCF10A-Er-Src	breast:	n/a	chr6:26034151-26034160
3	TAF1	chr6:26034242-26034625	K562	blood:	n/a	n/a
4	RCOR1	chr6:26033357-26034654	K562	blood:	n/a	n/a
5	GTF3C2	chr6:26034148-26034533	K562	blood:	n/a	n/a
6	CEBPD	chr6:26029286-26034640	K562	blood:	n/a	n/a
7	CHD1	chr6:26030593-26034261	H1-hESC	embryonic stem cell:	n/a	n/a
8	NR2F2	chr6:26030007-26034696	K562	blood:	n/a	n/a
9	MYBL2	chr6:26031451-26034257	HepG2	liver:	n/a	chr6:26031699-26031709
10	TCF12	chr6:26032911-26034404	SK-N-SH	brain:	n/a	n/a
11	SP1	chr6:26033111-26034747	HCT-116	colon:	n/a	chr6:26033924-26033945
12	CEBPB	chr6:26031391-26034289	GM12878	blood:	n/a	n/a
13	POLR2A	chr6:26031008-26034306	GM12878	blood:	n/a	n/a
14	POLR2A	chr6:26025305-26034609	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr6:26033485-26034404	GM12878	blood:	n/a	n/a
16	RUNX3	chr6:26031395-26034651	GM12878	blood:	n/a	n/a
17	TRIM28	chr6:26031407-26034348	K562	blood:	n/a	n/a
18	SETDB1	chr6:26033730-26034317	U2OS	brain:	n/a	n/a
19	HEY1	chr6:26024804-26034728	K562	blood:	n/a	chr6:26026612-26026621 chr6:26032481-26032490 chr6:26026610-26026619
20	CREB1	chr6:26031394-26034484	GM12878	blood:	n/a	chr6:26032480-26032493
21	BHLHE40	chr6:26033360-26034567	K562	blood:	n/a	n/a
22	MYBL2	chr6:26031291-26034345	HepG2	liver:	n/a	chr6:26031699-26031709
23	ZBTB33	chr6:26031402-26034523	SK-N-SH	brain:	n/a	chr6:26033544-26033559
24	MAX	chr6:26034049-26034648	K562	blood:	n/a	chr6:26034151-26034160
25	MTA3	chr6:26031232-26034583	GM12878	blood:	n/a	n/a
26	STAT3	chr6:26033764-26034593	MCF10A-Er-Src	breast:	n/a	n/a
27	NFIC	chr6:26033010-26034390	GM12878	blood:	n/a	n/a
28	EP300	chr6:26033227-26034396	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr6:26030199-26035426	MCF-7	breast:	n/a	n/a
30	JUND	chr6:26031440-26034435	HCT-116	colon:	n/a	chr6:26033077-26033086 chr6:26034150-26034159 chr6:26033905-26033914 chr6:26034089-26034096 chr6:26032482-26032491 chr6:26034152-26034163
31	MAX	chr6:26032031-26034445	NB4	blood:	n/a	chr6:26034151-26034160
32	FOS	chr6:26033955-26034512	HUVEC	blood vessel:	n/a	chr6:26034150-26034159 chr6:26034089-26034096 chr6:26034149-26034160 chr6:26034152-26034163
33	EGR1	chr6:26033625-26034836	HCT-116	colon:	n/a	chr6:26034443-26034457 chr6:26034487-26034501
34	STAT1	chr6:26033713-26034262	GM12878	blood:	n/a	n/a
35	SP1	chr6:26033507-26034259	H1-hESC	embryonic stem cell:	n/a	chr6:26033924-26033945
36	EGR1	chr6:26034203-26034635	K562	blood:	n/a	chr6:26034443-26034457 chr6:26034487-26034501
37	CEBPB	chr6:26033829-26034316	A549	lung:	n/a	n/a
38	PML	chr6:26030015-26034696	K562	blood:	n/a	n/a
39	ZEB1	chr6:26031408-26034436	HepG2	liver:	n/a	n/a
40	NFIC	chr6:26032856-26034275	SK-N-SH	brain:	n/a	n/a
41	POLR2A	chr6:26030171-26034714	K562	blood:	n/a	n/a
42	POLR2A	chr6:26032700-26034284	HUVEC	blood vessel:	n/a	n/a
43	NFIC	chr6:26030957-26034619	GM12878	blood:	n/a	n/a
44	EP300	chr6:26033703-26034719	K562	blood:	n/a	n/a
45	RUNX3	chr6:26031455-26034756	GM12878	blood:	n/a	n/a
46	SIN3AK20	chr6:26031464-26034667	HCT-116	colon:	n/a	n/a
47	STAT3	chr6:26033804-26034441	MCF10A-Er-Src	breast:	n/a	n/a
48	MEF2A	chr6:26033473-26034271	SK-N-SH	brain:	n/a	chr6:26034151-26034159 chr6:26034038-26034054
49	POLR2A	chr6:26030256-26034277	PANC-1	pancreas:	n/a	n/a
50	FOS	chr6:26033848-26034296	MCF10A-Er-Src	breast:	n/a	chr6:26034150-26034159 chr6:26033905-26033914 chr6:26034089-26034096 chr6:26034149-26034160 chr6:26034152-26034163

No.	Distal block	Cell Line	Cell type
1	chr6:26024607..26035097-chr6:27857610..27864739,17	K562	blood:
2	chr6:26030558..26034410-chr6:27100755..27103505,3	MCF-7	breast:
3	chr6:26032840..26034621-chr6:27775962..27778239,2	MCF-7	breast:
4	chr6:26032281..26034912-chr6:151976877..151979649,2	MCF-7	breast:
5	chr6:26030891..26034608-chr6:26223354..26228378,6	MCF-7	breast:
6	chr6:26017750..26036418-chr6:26116875..26130553,65	MCF-7	breast:
7	chr6:26033910..26036420-chr6:26515231..26517508,2	K562	blood:
8	chr6:26032417..26034288-chr6:27803614..27806340,2	K562	blood:
9	chr6:26029982..26034393-chr6:27104962..27111668,7	K562	blood:
10	chr6:26033420..26034983-chr6:43738377..43740879,2	MCF-7	breast:
11	chr1:11968743..11971201-chr6:26031885..26034451,2	MCF-7	breast:
12	chr6:26032382..26034370-chr6:27099704..27101484,2	MCF-7	breast:
13	chr6:26033297..26035200-chr6:27833856..27836117,3	MCF-7	breast:
14	chr6:26024161..26035534-chr6:27093020..27104638,25	K562	blood:
15	chr6:26031607..26034880-chr6:27837430..27841431,3	K562	blood:
16	chr6:26033333..26034270-chr6:26043612..26044453,2	NB4	blood:
17	chr6:26033712..26035752-chr6:27832969..27835289,2	MCF-7	breast:
18	chr6:26026115..26036040-chr6:27097153..27104835,26	K562	blood:
19	chr6:26032854..26035580-chr6:26251207..26253979,3	MCF-7	breast:
20	chr11:119205209..119206051-chr6:26033654..26034253,2	Hela-S3	cervix:
21	chr6:26019525..26036768-chr6:26154463..26163826,38	MCF-7	breast:
22	chr6:26030074..26034864-chr6:27112849..27118591,14	K562	blood:
23	chr6:26031804..26034805-chr6:26202147..26206144,5	MCF-7	breast:
24	chr6:26032234..26034590-chr6:26239058..26240623,2	MCF-7	breast:
25	chr6:26030021..26034897-chr6:26196138..26201230,10	MCF-7	breast:
26	chr6:26032288..26035408-chr6:26183846..26189517,7	MCF-7	breast:
27	chr6:26025629..26034912-chr6:27111740..27118591,16	K562	blood:

Variant related genes	Relation type
HIST1H2AB	TF binding region
HIST1H3B	TF binding region
ENSG00000198327	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000196966	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000197697	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000091831	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000217275	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000173456	Chromatin interaction
ENSG00000112715	Chromatin interaction
ENSG00000184357	Chromatin interaction
ENSG00000198339	Chromatin interaction
ENSG00000184348	Chromatin interaction
ENSG00000201801	Chromatin interaction
ENSG00000182572	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000197459	Chromatin interaction
ENSG00000198374	Chromatin interaction
ENSG00000198558	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000234816	Chromatin interaction
ENSG00000196226	Chromatin interaction
ENSG00000198518	Chromatin interaction
ENSG00000188987	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000203813	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10484434	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11751732	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11755492	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11756400	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11758378	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11759668	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11961143	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11965426	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2051538	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2230654	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34956419	0.92[ASN][1000 genomes]
rs36125084	0.81[AMR][1000 genomes]
rs3799374	0.92[ASN][1000 genomes]
rs41266783	0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55661658	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56073264	0.92[ASN][1000 genomes]
rs59281021	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61289224	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62000984	0.92[EUR][1000 genomes]
rs62394540	0.84[EUR][1000 genomes]
rs62394542	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62394555	0.92[ASN][1000 genomes]
rs62394556	0.92[ASN][1000 genomes]
rs62396160	0.92[ASN][1000 genomes]
rs62396164	0.92[ASN][1000 genomes]
rs66505449	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66536062	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6906460	0.80[EUR][1000 genomes]
rs6925912	0.80[EUR][1000 genomes]
rs6935470	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7757646	0.92[ASN][1000 genomes]
rs9689245	0.97[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	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers 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 target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers 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	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
11	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
12	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
13	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
14	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
15	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
16	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
17	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
18	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
19	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
20	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
21	nsv1026692	chr6:26027408-26067081	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	363 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs62394550	TRIM38	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26030200-26035000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr6:26030400-26034800	Active TSS	H9 Cell Line	embryonic stem cell
3	chr6:26030600-26034400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:26030600-26034400	Active TSS	A549	lung
5	chr6:26030600-26034600	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr6:26030800-26034400	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr6:26030800-26034600	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr6:26030800-26034600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:26030800-26034600	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr6:26030800-26034600	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr6:26030800-26035000	Active TSS	H1 Cell Line	embryonic stem cell
12	chr6:26031000-26034600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:26031000-26034600	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr6:26031200-26034400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr6:26031200-26034400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:26031200-26034600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr6:26031200-26034600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr6:26031200-26034600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:26031200-26034600	Active TSS	Dnd41	blood
20	chr6:26031200-26034800	Active TSS	Brain Germinal Matrix	brain
21	chr6:26031400-26034800	Flanking Active TSS	HUVEC	blood vessel
22	chr6:26031600-26034400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:26031600-26034400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:26031600-26034400	Active TSS	Colonic Mucosa	Colon
25	chr6:26031600-26034600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr6:26031600-26034600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr6:26031800-26034400	Active TSS	Right Ventricle	heart
28	chr6:26031800-26034400	Active TSS	Sigmoid Colon	Sigmoid Colon
29	chr6:26031800-26034600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr6:26031800-26034600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr6:26031800-26034600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
32	chr6:26031800-26034600	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr6:26032000-26034400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr6:26032000-26034400	Active TSS	Small Intestine	intestine
35	chr6:26032000-26034600	Active TSS	Brain Angular Gyrus	brain
36	chr6:26032000-26034600	Active TSS	Brain Substantia Nigra	brain
37	chr6:26032000-26034600	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr6:26032000-26034800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:26032200-26034400	Active TSS	Esophagus	oesophagus
40	chr6:26032200-26034400	Active TSS	Placenta Amnion	Placenta Amnion
41	chr6:26032200-26034400	Active TSS	Stomach Mucosa	stomach
42	chr6:26032400-26034400	Active TSS	Aorta	Aorta
43	chr6:26032600-26034600	Flanking Active TSS	Fetal Muscle Leg	muscle
44	chr6:26032600-26034800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr6:26032600-26034800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr6:26032800-26034400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr6:26033000-26034400	Active TSS	NHDF-Ad	bronchial
48	chr6:26033200-26034400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:26033200-26034400	Active TSS	Fetal Kidney	kidney
50	chr6:26033200-26034400	Active TSS	Rectal Mucosa Donor 31	rectum

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