Variant report

Variant	rs67575965
Chromosome Location	chr6:26196593-26196594
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26195405-26197856	GM12891	blood:	n/a	n/a
2	POLR2A	chr6:26195569-26197730	GM19099	blood:	n/a	n/a
3	POLR2A	chr6:26193825-26201103	K562	blood:	n/a	n/a
4	EGR1	chr6:26196495-26196957	K562	blood:	n/a	n/a
5	BCLAF1	chr6:26196446-26197944	GM12878	blood:	n/a	n/a
6	POLR2A	chr6:26187684-26208312	K562	blood:	n/a	n/a
7	RELA	chr6:26196586-26197686	GM15510	blood:	n/a	n/a
8	POLR2A	chr6:26195351-26200889	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr6:26195529-26197821	HepG2	liver:	n/a	n/a
10	ATF2	chr6:26194955-26200949	H1-hESC	embryonic stem cell:	n/a	n/a
11	USF1	chr6:26196100-26196600	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr6:26192611-26200894	K562	blood:	n/a	n/a
13	POLR2A	chr6:26195442-26197906	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr6:26195420-26197887	GM12892	blood:	n/a	n/a
15	POLR2A	chr6:26196491-26197742	HepG2	liver:	n/a	n/a
16	POLR2A	chr6:26196587-26200011	MCF10A-Er-Src	breast:	n/a	n/a
17	CEBPD	chr6:26196481-26196789	HepG2	liver:	n/a	n/a
18	YY1	chr6:26196203-26196718	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:26196484-26197846	HepG2	liver:	n/a	n/a
20	POLR2A	chr6:26195642-26197728	GM18951	blood:	n/a	n/a
21	POLR2A	chr6:26195511-26197839	HUVEC	blood vessel:	n/a	n/a
22	POU2F2	chr6:26195495-26197894	GM12878	blood:	n/a	chr6:26196504-26196512
23	MTA3	chr6:26196223-26197885	GM12878	blood:	n/a	n/a
24	FOXM1	chr6:26196049-26198123	GM12878	blood:	n/a	n/a
25	USF1	chr6:26196075-26196697	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr6:26195423-26197907	HepG2	liver:	n/a	n/a
27	HEY1	chr6:26196077-26197797	HepG2	liver:	n/a	n/a
28	CREB1	chr6:26195402-26197980	HepG2	liver:	n/a	chr6:26197774-26197787
29	POLR2A	chr6:26195548-26200603	U87	brain:	n/a	n/a
30	MAX	chr6:26196203-26196798	Hela-S3	cervix:	n/a	n/a
31	PML	chr6:26193184-26200952	K562	blood:	n/a	n/a
32	ZNF384	chr6:26195363-26196694	GM12878	blood:	n/a	n/a
33	CTCF	chr6:26196580-26196730	BE2_C	brain:	n/a	n/a
34	TAF7	chr6:26194455-26200989	H1-hESC	embryonic stem cell:	n/a	n/a
35	TEAD4	chr6:26193268-26200973	K562	blood:	n/a	n/a
36	POLR2A	chr6:26195635-26197691	GM18526	blood:	n/a	n/a
37	USF1	chr6:26196127-26196655	HCT-116	colon:	n/a	n/a
38	USF2	chr6:26195553-26197683	Hela-S3	cervix:	n/a	chr6:26196355-26196366
39	NFIC	chr6:26195431-26200718	GM12878	blood:	n/a	chr6:26195653-26195669
40	POLR2A	chr6:26195432-26197773	GM12891	blood:	n/a	n/a
41	CHD2	chr6:26196589-26196822	GM12878	blood:	n/a	n/a
42	POLR2A	chr6:26195341-26200934	HL-60	blood:	n/a	n/a
43	WRNIP1	chr6:26196523-26197784	GM12878	blood:	n/a	n/a
44	MXI1	chr6:26196392-26196708	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr6:26195530-26197759	K562	blood:	n/a	n/a
46	CEBPB	chr6:26196341-26197994	GM12878	blood:	n/a	n/a
47	POLR2A	chr6:26195499-26197893	GM12892	blood:	n/a	n/a
48	POLR2A	chr6:26195326-26200683	GM12878	blood:	n/a	n/a
49	NFIC	chr6:26196176-26197976	GM12878	blood:	n/a	n/a
50	RUNX3	chr6:26195557-26197678	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26196580-26196630	U87	brain:	n/a
2	chr6:26196580-26196630	A549	lung:	n/a
3	chr6:26196580-26196630	GM06990	blood:	n/a
4	chr6:26196580-26196630	HCF	heart:	n/a
5	chr6:26196580-26196630	HUVEC	blood vessel:	n/a
6	chr6:26196580-26196630	GM12892	blood:	n/a
7	chr6:26196580-26196630	HCT-116	colon:	n/a
8	chr6:26196580-26196630	GM12891	blood:	n/a
9	chr6:26196580-26196630	Caco-2	colon:	n/a
10	chr6:26196580-26196630	SK-N-SH	brain:	n/a
11	chr6:26196580-26196630	AG09309	skin:	n/a
12	chr6:26196580-26196630	SK-N-SH_RA	brain:	n/a
13	chr6:26196580-26196630	BE2_C	brain:	n/a
14	chr6:26196580-26196630	BJ	skin:	n/a
15	chr6:26196580-26196630	HL-60	blood:	n/a
16	chr6:26196580-26196630	HRPEpiC	eye:	n/a
17	chr6:26196580-26196630	HEK293	kidney:	embryo
18	chr6:26196580-26196630	PANC-1	pancreas:	n/a
19	chr6:26196580-26196630	HepG2	liver:	n/a
20	chr6:26196580-26196630	ovcar-3	ovarian:	n/a
21	chr6:26196580-26196630	HCPEpiC	choroid plexus:	n/a
22	chr6:26196580-26196630	PFSK-1	brain:	n/a
23	chr6:26196580-26196630	SK-N-MC	brain:	n/a
24	chr6:26196580-26196630	AG09319	gingival:	n/a
25	chr6:26196580-26196630	HRE	kidney:	n/a
26	chr6:26196580-26196630	T-47D	breast:	n/a
27	chr6:26196580-26196630	NHDF-neo	bronchial:	n/a
28	chr6:26196580-26196630	HRCEpiC	kidney:	n/a
29	chr6:26196580-26196630	Hela-S3	cervix:	n/a
30	chr6:26196580-26196630	MCF10A-Er-Src	breast:	n/a
31	chr6:26196580-26196630	SAEC	small airway:	n/a
32	chr6:26196580-26196630	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:26196580-26196630	NH-A	brain:	n/a
34	chr6:26196580-26196630	NHBE	bronchial:	n/a
35	chr6:26196580-26196630	AG04449	skin:	fetal
36	chr6:26196580-26196630	AoSMC	blood vessel:	n/a
37	chr6:26196580-26196630	Hepatocyte	liver:	n/a
38	chr6:26196580-26196630	HMEC	breast:	n/a
39	chr6:26196580-26196630	SKMC	muscle:	n/a
40	chr6:26196580-26196630	HAEpiC	amniotic membrane:	n/a
41	chr6:26196580-26196630	AG04450	lung:	fetal
42	chr6:26196580-26196630	CMK	blood:	n/a
43	chr6:26196580-26196630	HEEpiC	esophagus:	n/a
44	chr6:26196580-26196630	IMR90	lung:	fetal
45	chr6:26196580-26196630	HNPCEpiC	eye:	n/a
46	chr6:26196580-26196630	NT2-D1	testis:	n/a
47	chr6:26196580-26196630	GM19239	blood:	n/a
48	chr6:26196580-26196630	LNCaP	prostate:	n/a
49	chr6:26196580-26196630	NB4	blood:	n/a
50	chr6:26196580-26196630	ProgFib	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:57466580..57468767-chr6:26193927..26196753,2	K562	blood:
2	chr6:26045359..26046880-chr6:26195813..26197342,2	MCF-7	breast:
3	chr6:26196435..26200575-chr6:27099094..27104350,6	MCF-7	breast:
4	chr3:161089431..161091438-chr6:26196434..26199354,2	MCF-7	breast:
5	chr6:26020982..26024830-chr6:26195555..26199073,5	MCF-7	breast:
6	chr6:26030021..26034897-chr6:26196138..26201230,10	MCF-7	breast:
7	chr6:26196016..26198386-chr6:26419404..26421954,3	K562	blood:
8	chr6:26193858..26202011-chr6:27112529..27117825,14	K562	blood:
9	chr6:26195075..26199998-chr6:26518402..26523264,7	K562	blood:
10	chr6:26195729..26208268-chr6:27092660..27105612,50	K562	blood:
11	chr6:26195849..26201222-chr6:27858647..27864324,7	K562	blood:
12	chr6:26196234..26202173-chr6:27109710..27116918,20	K562	blood:
13	chr1:147806662..147807285-chr6:26196419..26197255,2	Hela-S3	cervix:
14	chr6:26195787..26199567-chr6:27858679..27862629,4	MCF-7	breast:
15	chr1:145382340..145383089-chr6:26196467..26197208,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
HIST1H2BF	TF binding region
HIST1H2BF	CpG island
ENSG00000201558	Chromatin interaction
ENSG00000196532	Chromatin interaction
ENSG00000087460	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000124549	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000196542	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000202408	Chromatin interaction
ENSG00000233396	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10452600	0.81[ASN][1000 genomes]
rs11754744	0.81[ASN][1000 genomes]
rs11755210	0.81[ASN][1000 genomes]
rs11755943	0.82[ASN][1000 genomes]
rs11757394	0.81[ASN][1000 genomes]
rs11758351	1.00[ASN][1000 genomes]
rs1341759	0.81[ASN][1000 genomes]
rs16891397	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16891401	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16891405	0.81[ASN][1000 genomes]
rs1997768	0.82[ASN][1000 genomes]
rs2022448	0.81[ASN][1000 genomes]
rs2069018	0.81[ASN][1000 genomes]
rs2069019	0.81[ASN][1000 genomes]
rs2069020	0.81[ASN][1000 genomes]
rs2143346	0.81[ASN][1000 genomes]
rs2183948	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3734533	0.81[ASN][1000 genomes]
rs3757135	0.81[ASN][1000 genomes]
rs41266801	0.81[ASN][1000 genomes]
rs41266807	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs55815656	0.81[ASN][1000 genomes]
rs56186759	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 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	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
17	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
18	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
19	nsv883490	chr6:26172219-26231608	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	316 gene(s)	inside rSNPs	diseases
20	nsv1021294	chr6:26190316-26246784	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	309 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	chr6:26193600-26198400	Transcr. at gene 5' and 3'	K562	blood
2	chr6:26194200-26200600	Active TSS	GM12878-XiMat	blood
3	chr6:26194600-26196800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:26194800-26196600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr6:26194800-26197200	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr6:26194800-26199800	Active TSS	Duodenum Smooth Muscle	Duodenum
7	chr6:26194800-26201000	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr6:26195000-26196600	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr6:26195000-26196600	Active TSS	Brain Hippocampus Middle	brain
10	chr6:26195000-26197000	Active TSS	Brain Anterior Caudate	brain
11	chr6:26195000-26197200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:26195000-26197800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:26195000-26199800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:26195000-26200400	Active TSS	Aorta	Aorta
15	chr6:26195000-26200400	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr6:26195000-26200600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr6:26195000-26200800	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr6:26195000-26200800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr6:26195000-26200800	Active TSS	NHDF-Ad	bronchial
20	chr6:26195200-26196600	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr6:26195200-26196600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:26195200-26196600	Active TSS	Colon Smooth Muscle	Colon
23	chr6:26195200-26196600	Active TSS	Right Atrium	heart
24	chr6:26195200-26196800	Active TSS	Brain Cingulate Gyrus	brain
25	chr6:26195200-26196800	Active TSS	Rectal Smooth Muscle	rectum
26	chr6:26195200-26197000	Active TSS	Fetal Brain Female	brain
27	chr6:26195200-26197600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:26195200-26197600	Active TSS	Ovary	ovary
29	chr6:26195200-26200000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr6:26195200-26200000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr6:26195200-26200000	Active TSS	NHLF	lung
32	chr6:26195200-26200600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:26195200-26200600	Active TSS	Brain Angular Gyrus	brain
34	chr6:26195200-26200800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr6:26195200-26201000	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr6:26195200-26201400	Active TSS	H1 Cell Line	embryonic stem cell
37	chr6:26195400-26196600	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr6:26195400-26196600	Active TSS	Colonic Mucosa	Colon
39	chr6:26195400-26196600	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr6:26195400-26196600	Active TSS	HepG2	liver
41	chr6:26195400-26196800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:26195400-26196800	Active TSS	Stomach Mucosa	stomach
43	chr6:26195400-26197200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr6:26195400-26197800	Bivalent/Poised TSS	Psoas Muscle	Psoas
45	chr6:26195400-26198000	Active TSS	Primary T cells from cord blood	blood
46	chr6:26195400-26199000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr6:26195400-26199800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr6:26195400-26199800	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr6:26195400-26199800	Active TSS	Fetal Kidney	kidney
50	chr6:26195400-26200000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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