Variant report

Variant	rs2242655
Chromosome Location	chr6:31627449-31627450
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:94)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:94 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	REST	chr6:31627391-31627732	A549	lung:	n/a	n/a
2	POLR2A	chr6:31624845-31631075	K562	blood:	n/a	n/a
3	REST	chr6:31627433-31627799	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr6:31627402-31629138	GM12878	blood:	n/a	n/a
5	YY1	chr6:31627323-31627900	K562	blood:	n/a	n/a
6	HEY1	chr6:31627241-31629259	K562	blood:	n/a	chr6:31628563-31628578
7	NR2F2	chr6:31627008-31629425	K562	blood:	n/a	n/a
8	TEAD4	chr6:31627357-31629173	K562	blood:	n/a	n/a
9	SIN3AK20	chr6:31627436-31627851	SK-N-SH	brain:	n/a	n/a
10	TEAD4	chr6:31627435-31627921	A549	lung:	n/a	n/a
11	REST	chr6:31627335-31627901	U87	brain:	n/a	n/a
12	REST	chr6:31627355-31627957	ECC-1	luminal epithelium:	n/a	n/a
13	ELF1	chr6:31627409-31628899	SK-N-SH	brain:	n/a	chr6:31628049-31628062
14	TEAD4	chr6:31625264-31629276	K562	blood:	n/a	n/a
15	GABPA	chr6:31627408-31628833	K562	blood:	n/a	n/a
16	POLR2A	chr6:31627428-31628826	GM12891	blood:	n/a	n/a
17	ELF1	chr6:31627085-31627825	GM12878	blood:	n/a	n/a
18	PML	chr6:31627400-31629252	K562	blood:	n/a	n/a
19	ELF1	chr6:31626778-31629307	K562	blood:	n/a	chr6:31628049-31628062
20	POLR2A	chr6:31627364-31629088	HL-60	blood:	n/a	n/a
21	REST	chr6:31627404-31627837	SK-N-SH	brain:	n/a	n/a
22	REST	chr6:31627248-31628091	MCF-7	breast:	n/a	n/a
23	POLR2A	chr6:31626649-31630457	K562	blood:	n/a	n/a
24	STAT5A	chr6:31627064-31629183	GM12878	blood:	n/a	chr6:31627992-31628006 chr6:31628822-31628830 chr6:31628864-31628876
25	MTA3	chr6:31627079-31629236	GM12878	blood:	n/a	n/a
26	MAX	chr6:31626859-31629268	K562	blood:	n/a	n/a
27	ELF1	chr6:31627355-31627748	HepG2	liver:	n/a	n/a
28	REST	chr6:31627254-31628702	HL-60	blood:	n/a	n/a
29	REST	chr6:31627447-31627746	PANC-1	pancreas:	n/a	n/a
30	POLR2A	chr6:31624936-31630633	HepG2	liver:	n/a	n/a
31	REST	chr6:31627316-31628762	MCF-7	breast:	n/a	n/a
32	TAF1	chr6:31627270-31628974	K562	blood:	n/a	n/a
33	POLR2A	chr6:31624880-31629304	K562	blood:	n/a	n/a
34	SIN3AK20	chr6:31627064-31629219	K562	blood:	n/a	n/a
35	POLR2A	chr6:31624853-31630685	HepG2	liver:	n/a	n/a
36	POLR2A	chr6:31626622-31629281	HepG2	liver:	n/a	n/a
37	POLR2A	chr6:31626608-31630297	K562	blood:	n/a	n/a
38	REST	chr6:31627351-31627884	PFSK-1	brain:	n/a	n/a
39	POLR2A	chr6:31627442-31628746	GM12878	blood:	n/a	n/a
40	ELF1	chr6:31627434-31628798	GM12878	blood:	n/a	chr6:31628049-31628062
41	POLR2A	chr6:31627418-31627581	HepG2	liver:	n/a	n/a
42	POLR2A	chr6:31626521-31628936	GM12878	blood:	n/a	n/a
43	REST	chr6:31627335-31627960	H1-hESC	embryonic stem cell:	n/a	n/a
44	IRF1	chr6:31627438-31629092	K562	blood:	n/a	chr6:31628085-31628092 chr6:31628567-31628581
45	POLR2A	chr6:31627439-31627466	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr6:31626356-31629360	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr6:31624894-31629292	K562	blood:	n/a	n/a
48	POLR2A	chr6:31627081-31629182	K562	blood:	n/a	n/a
49	POLR2A	chr6:31627417-31629320	GM12892	blood:	n/a	n/a
50	REST	chr6:31627306-31627871	HepG2	liver:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31627130..31628975-chr6:32096561..32099431,2	K562	blood:
2	chr6:31506029..31511048-chr6:31626239..31630287,7	MCF-7	breast:
3	chr6:31626696..31628687-chr6:31762053..31764771,3	MCF-7	breast:
4	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
5	chr6:31495999..31499455-chr6:31625533..31627883,4	K562	blood:
6	chr6:31625699..31629901-chr6:31762894..31764968,3	MCF-7	breast:
7	chr6:31586074..31595285-chr6:31626460..31635395,11	MCF-7	breast:
8	chr6:31508417..31511292-chr6:31625631..31629953,4	K562	blood:
9	chr6:31627002..31627882-chr9:128003181..128003743,2	Hela-S3	cervix:
10	chr6:31626044..31628862-chr6:31901843..31903585,2	K562	blood:
11	chr12:109123761..109125995-chr6:31627199..31629495,2	MCF-7	breast:
12	chr6:31626203..31628838-chr6:31668692..31672480,4	MCF-7	breast:
13	chr6:31626270..31630199-chr6:31829030..31832230,7	K562	blood:
14	chr6:31626011..31627858-chr6:31773563..31776349,2	MCF-7	breast:
15	chr6:31509627..31511469-chr6:31626737..31628735,4	MCF-7	breast:
16	chr19:47287460..47289701-chr6:31626637..31629167,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000201207	TF binding region
ENSG00000198563	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000266776	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204315	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000105281	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000044574	Chromatin interaction
ENSG00000110880	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000204511	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12524536	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12525100	0.80[ASN][1000 genomes]
rs12529661	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16899941	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2077102	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2242653	0.98[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2242657	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2242658	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2269475	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2280800	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2295664	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2295665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28366149	0.85[ASN][1000 genomes]
rs28474889	0.86[ASN][1000 genomes]
rs3763295	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs41267070	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4711274	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56826489	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59345959	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6927872	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs760294	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
3	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
5	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
7	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
9	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
10	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
11	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
12	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
13	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
14	nsv462871	chr6:31575276-31632134	Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
15	nsv601942	chr6:31575276-31632134	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
16	nsv884419	chr6:31585000-31632651	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
17	nsv884420	chr6:31586827-31632651	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
18	nsv884421	chr6:31588151-31631907	Active TSS Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	129 gene(s)	inside rSNPs	diseases
19	nsv884422	chr6:31592524-31631907	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
20	nsv884424	chr6:31593729-31632651	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
21	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
22	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2242655	CCHCR1	cis	lymphoblastoid	seeQTL
rs2242655	C6orf48	cis	multi-tissue	Pritchard
rs2242655	AIF1	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31621400-31627600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:31621400-31627600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:31626000-31627800	Enhancers	Fetal Brain Male	brain
4	chr6:31626000-31628200	Flanking Active TSS	K562	blood
5	chr6:31626200-31628000	Flanking Active TSS	Hela-S3	cervix
6	chr6:31626200-31628200	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr6:31626200-31628400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr6:31626200-31628400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr6:31626400-31628400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:31626600-31627800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
11	chr6:31626600-31628000	Flanking Active TSS	Brain Germinal Matrix	brain
12	chr6:31626600-31628000	Flanking Active TSS	Rectal Smooth Muscle	rectum
13	chr6:31626600-31628200	Flanking Active TSS	Fetal Brain Female	brain
14	chr6:31626600-31628200	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
15	chr6:31626600-31628200	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr6:31626600-31628400	Transcr. at gene 5' and 3'	Dnd41	blood
17	chr6:31626800-31627600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:31626800-31627600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr6:31626800-31627600	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
20	chr6:31626800-31627600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr6:31626800-31627600	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
22	chr6:31626800-31627600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:31626800-31627600	Flanking Active TSS	Pancreas	Pancrea
24	chr6:31626800-31627600	Flanking Active TSS	Psoas Muscle	Psoas
25	chr6:31626800-31627600	Flanking Active TSS	HSMM	muscle
26	chr6:31626800-31627600	Flanking Active TSS	Osteobl	bone
27	chr6:31626800-31627800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:31626800-31627800	Flanking Active TSS	Colon Smooth Muscle	Colon
29	chr6:31626800-31627800	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
30	chr6:31626800-31628000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr6:31626800-31628000	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr6:31626800-31628000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr6:31626800-31628000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr6:31626800-31628200	Flanking Active TSS	Liver	Liver
35	chr6:31626800-31628200	Flanking Active TSS	Brain Cingulate Gyrus	brain
36	chr6:31626800-31628200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:31626800-31628200	Flanking Active TSS	NH-A	brain
38	chr6:31626800-31629000	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr6:31626800-31629000	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr6:31626800-31629200	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr6:31626800-31629200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr6:31626800-31629200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr6:31627000-31627600	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
44	chr6:31627000-31627600	Transcr. at gene 5' and 3'	Placenta	Placenta
45	chr6:31627000-31627600	Flanking Active TSS	NHEK	skin
46	chr6:31627000-31627800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:31627000-31627800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr6:31627000-31627800	Flanking Active TSS	Colonic Mucosa	Colon
49	chr6:31627000-31627800	Flanking Active TSS	Right Atrium	heart
50	chr6:31627000-31627800	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon

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