Variant report

Variant	rs2844472
Chromosome Location	chr6:31589676-31589677
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31589401-31590047	K562	blood:	n/a	n/a
2	POLR2A	chr6:31587351-31591130	GM12878	blood:	n/a	n/a
3	POLR2A	chr6:31587203-31590940	SK-N-MC	brain:	n/a	n/a
4	HEY1	chr6:31587125-31591017	K562	blood:	n/a	chr6:31588313-31588328 chr6:31588969-31588984
5	JUN	chr6:31587004-31589748	K562	blood:	n/a	chr6:31587856-31587869 chr6:31588931-31588945 chr6:31588001-31588010
6	MTA3	chr6:31587330-31589818	GM12878	blood:	n/a	n/a
7	TEAD4	chr6:31587224-31590369	K562	blood:	n/a	n/a
8	POLR2A	chr6:31587597-31590981	PANC-1	pancreas:	n/a	n/a
9	POLR2A	chr6:31587263-31591139	H1-hESC	embryonic stem cell:	n/a	n/a
10	WRNIP1	chr6:31589492-31590004	GM12878	blood:	n/a	n/a
11	CHD1	chr6:31588515-31589930	H1-hESC	embryonic stem cell:	n/a	chr6:31588728-31588738
12	PML	chr6:31587282-31589811	K562	blood:	n/a	n/a
13	REST	chr6:31587201-31589978	H1-neurons	neurons:	n/a	chr6:31588428-31588441 chr6:31588789-31588802 chr6:31589059-31589066
14	YY1	chr6:31589456-31589744	K562	blood:	n/a	n/a
15	MXI1	chr6:31587584-31590610	IMR90	lung:	n/a	n/a
16	POLR2A	chr6:31589551-31589788	Hela-S3	cervix:	n/a	n/a
17	RFX5	chr6:31587221-31590646	SK-N-SH	brain:	n/a	chr6:31588254-31588263
18	POLR2A	chr6:31587529-31589823	IMR90	lung:	n/a	n/a
19	POLR2A	chr6:31587431-31590006	PFSK-1	brain:	n/a	n/a
20	POLR2A	chr6:31589530-31590066	GM12891	blood:	n/a	n/a
21	POLR2A	chr6:31589321-31590143	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr6:31587447-31591084	GM12878	blood:	n/a	n/a
23	JUND	chr6:31587259-31589939	SK-N-SH	brain:	n/a	chr6:31588931-31588945 chr6:31588001-31588010
24	POLR2A	chr6:31587609-31589747	HepG2	liver:	n/a	n/a
25	POLR2A	chr6:31589373-31590243	PFSK-1	brain:	n/a	n/a
26	TAF1	chr6:31589277-31589754	K562	blood:	n/a	n/a
27	CHD1	chr6:31587340-31590171	IMR90	lung:	n/a	chr6:31588728-31588738

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31463965..31465758-chr6:31589334..31591777,2	K562	blood:
2	chr6:31586339..31592286-chr6:31830032..31833457,6	K562	blood:
3	chr6:31552844..31558545-chr6:31585940..31590373,6	MCF-7	breast:
4	chr6:30523103..30525725-chr6:31587969..31589968,2	MCF-7	breast:
5	chr6:31586197..31590294-chr6:31618213..31621899,10	MCF-7	breast:
6	chr6:31513053..31519210-chr6:31585987..31595406,29	K562	blood:
7	chr6:31506740..31512488-chr6:31586502..31592966,30	K562	blood:
8	chr6:31495666..31498592-chr6:31587530..31589995,2	K562	blood:
9	chr6:31511829..31516829-chr6:31586761..31590434,8	MCF-7	breast:
10	chr6:31587448..31589830-chr6:31773246..31774977,2	MCF-7	breast:
11	chr6:31499501..31502092-chr6:31587750..31590043,2	K562	blood:
12	chr6:31465865..31468194-chr6:31588116..31590521,2	K562	blood:
13	chr6:31463303..31465758-chr6:31589334..31591958,3	K562	blood:
14	chr6:31587709..31590301-chr6:31782411..31784104,4	MCF-7	breast:
15	chr6:31512646..31517552-chr6:31586243..31590655,20	K562	blood:
16	chr6:31507058..31511692-chr6:31586700..31590601,11	MCF-7	breast:
17	chr6:31547327..31550393-chr6:31586001..31589795,6	K562	blood:
18	chr6:31507082..31511713-chr6:31583957..31591905,17	MCF-7	breast:
19	chr6:31537778..31540136-chr6:31588503..31590021,2	MCF-7	breast:
20	chr6:31545892..31550426-chr6:31586652..31590237,7	MCF-7	breast:
21	chr6:31588069..31590107-chr6:31801555..31804354,2	MCF-7	breast:
22	chr6:31587809..31589938-chr6:32155791..32158478,2	K562	blood:
23	chr6:31586074..31595285-chr6:31626460..31635395,11	MCF-7	breast:
24	chr6:31587256..31589792-chr6:32936886..32939451,3	K562	blood:
25	chr6:31587689..31590254-chr6:32938301..32941446,3	MCF-7	breast:
26	chr6:31588260..31590209-chr6:31637745..31639673,2	MCF-7	breast:
27	chr6:31542086..31543755-chr6:31589416..31592351,2	K562	blood:
28	chr6:31506595..31512441-chr6:31585525..31590767,30	K562	blood:
29	chr6:31494785..31496809-chr6:31588128..31590003,2	K562	blood:
30	chr6:31546034..31550400-chr6:31586618..31591027,9	K562	blood:
31	chr6:31587220..31590773-chr6:31700977..31706290,6	MCF-7	breast:

No data

Variant related genes	Relation type
PRRC2A	TF binding region
SNORA38	TF binding region
ENSG00000226979	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204516	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000227507	Chromatin interaction
ENSG00000240053	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204482	Chromatin interaction
ENSG00000204392	Chromatin interaction
ENSG00000225499	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000232810	Chromatin interaction
ENSG00000204590	Chromatin interaction
ENSG00000201680	Chromatin interaction
ENSG00000263756	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204576	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204304	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204511	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1052486	0.90[ASN][1000 genomes]
rs1077393	0.90[ASN][1000 genomes]
rs13716	0.86[AMR][1000 genomes]
rs2051552	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2077491	0.88[ASN][1000 genomes]
rs2077492	0.82[ASN][1000 genomes]
rs2242659	0.81[ASN][1000 genomes]
rs2242660	0.82[ASN][1000 genomes]
rs2259571	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2260000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2260050	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2507957	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2736155	0.88[ASN][1000 genomes]
rs2736171	0.91[EUR][1000 genomes]
rs2736172	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736176	0.82[AMR][1000 genomes]
rs2736178	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2844465	0.81[ASN][1000 genomes]
rs2844475	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2844476	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2844477	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2857693	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2857694	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2857697	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2857698	0.82[AMR][1000 genomes]
rs3091280	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3135044	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3993747	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4569	0.80[ASN][1000 genomes]
rs5872	0.84[AMR][1000 genomes]
rs7029	0.80[ASN][1000 genomes]
rs707919	0.84[AMR][1000 genomes]
rs707920	0.80[ASN][1000 genomes]
rs755714	0.86[AMR][1000 genomes]
rs7765613	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7992	0.80[ASN][1000 genomes]
rs805262	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs805299	0.84[AMR][1000 genomes]
rs805301	0.81[ASN][1000 genomes]
rs805302	0.81[ASN][1000 genomes]
rs805303	0.83[ASN][1000 genomes]
rs813115	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 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

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2844472	PRRC2A	cis	lymphoblastoid	seeQTL
rs2844472	CSNK2B	Cis_1M	lymphoblastoid	RTeQTL
rs2844472	CSNK2B	cis	lymphoblastoid	seeQTL
rs2844472	AIF1	Cis_1M	lymphoblastoid	RTeQTL
rs2844472	HLA-DQB1	Cis_chr	lymphoblastoid	RTeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31587200-31589800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:31587200-31589800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:31587200-31589800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:31587200-31589800	Active TSS	Brain Germinal Matrix	brain
5	chr6:31587200-31589800	Active TSS	Psoas Muscle	Psoas
6	chr6:31587200-31590000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:31587200-31590000	Active TSS	HSMM	muscle
8	chr6:31587200-31590000	Active TSS	NHLF	lung
9	chr6:31587200-31590200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:31587400-31589800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:31587400-31589800	Active TSS	Aorta	Aorta
12	chr6:31587400-31589800	Active TSS	Fetal Kidney	kidney
13	chr6:31587400-31590000	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr6:31587400-31590000	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr6:31587400-31590200	Active TSS	H9 Cell Line	embryonic stem cell
16	chr6:31587400-31590200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:31587400-31590200	Active TSS	Right Ventricle	heart
18	chr6:31587400-31590200	Active TSS	NHDF-Ad	bronchial
19	chr6:31587400-31590400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:31587600-31589800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr6:31587600-31590000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr6:31587600-31590000	Active TSS	Brain Angular Gyrus	brain
23	chr6:31587800-31590000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr6:31587800-31590000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:31587800-31590000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:31587800-31590000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:31587800-31590000	Active TSS	Gastric	stomach
28	chr6:31587800-31590200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:31588600-31590200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
30	chr6:31588800-31589800	Flanking Active TSS	Primary B cells from cord blood	blood
31	chr6:31588800-31589800	Active TSS	Right Atrium	heart
32	chr6:31588800-31590200	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr6:31588800-31590400	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr6:31588800-31591000	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
35	chr6:31589000-31589800	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr6:31589000-31589800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr6:31589000-31589800	Flanking Active TSS	Liver	Liver
38	chr6:31589000-31590200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:31589000-31590400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:31589000-31590600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr6:31589000-31590600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr6:31589000-31591000	Transcr. at gene 5' and 3'	Dnd41	blood
43	chr6:31589200-31589800	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr6:31589200-31589800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr6:31589200-31590000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr6:31589200-31590200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr6:31589200-31590200	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr6:31589200-31590200	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr6:31589200-31590600	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr6:31589200-31590800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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