Variant report

Variant	rs10947088
Chromosome Location	chr6:30709830-30709831
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:197)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:197 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SMARCB1	chr6:30707405-30712696	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr6:30709185-30711328	SK-N-SH	brain:	n/a	n/a
3	POLR2A	chr6:30709183-30712741	K562	blood:	n/a	n/a
4	POLR2A	chr6:30709565-30712522	GM18505	blood:	n/a	n/a
5	POLR2A	chr6:30709673-30711353	A549	lung:	n/a	n/a
6	POLR2A	chr6:30704670-30712656	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr6:30708838-30712666	HUVEC	blood vessel:	n/a	n/a
8	POLR2A	chr6:30708868-30712745	HCT-116	colon:	n/a	n/a
9	ZNF143	chr6:30709335-30711398	Hela-S3	cervix:	n/a	chr6:30710926-30710944
10	MXI1	chr6:30709821-30710933	GM12878	blood:	n/a	n/a
11	POLR2A	chr6:30707434-30712732	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr6:30707893-30713121	HepG2	liver:	n/a	n/a
13	MYBL2	chr6:30709493-30712702	HepG2	liver:	n/a	n/a
14	RAD21	chr6:30709386-30712657	HCT-116	colon:	n/a	chr6:30712416-30712429 chr6:30710226-30710239 chr6:30712391-30712405
15	SIN3AK20	chr6:30709484-30712745	HCT-116	colon:	n/a	n/a
16	MBD4	chr6:30709584-30712628	HepG2	liver:	n/a	n/a
17	POLR2A	chr6:30709594-30712532	GM19193	blood:	n/a	n/a
18	SIN3AK20	chr6:30709089-30712768	HCT-116	colon:	n/a	n/a
19	CBX3	chr6:30709702-30712696	HCT-116	colon:	n/a	n/a
20	GATA3	chr6:30709695-30711537	A549	lung:	n/a	n/a
21	POLR2A	chr6:30709480-30711719	HepG2	liver:	n/a	n/a
22	TCF12	chr6:30709232-30712934	A549	lung:	n/a	chr6:30710631-30710641
23	POLR2A	chr6:30709477-30711350	GM12878	blood:	n/a	n/a
24	FOXM1	chr6:30709789-30710996	GM12878	blood:	n/a	n/a
25	POLR2A	chr6:30709408-30712678	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr6:30709572-30712537	GM18951	blood:	n/a	n/a
27	GATA3	chr6:30709630-30711359	A549	lung:	n/a	n/a
28	SP1	chr6:30709444-30712767	HCT-116	colon:	n/a	chr6:30710465-30710476 chr6:30710688-30710697 chr6:30712384-30712395 chr6:30710287-30710301 chr6:30710687-30710699 chr6:30710689-30710698 chr6:30710850-30710857 chr6:30710288-30710297 chr6:30710527-30710536 chr6:30710526-30710538 chr6:30710526-30710538 chr6:30710532-30710539 chr6:30710687-30710699 chr6:30710502-30710513 chr6:30710526-30710537
29	POLR2A	chr6:30708940-30712572	Hela-S3	cervix:	n/a	n/a
30	TFAP2C	chr6:30709511-30711204	Hela-S3	cervix:	n/a	n/a
31	BCL3	chr6:30709602-30711567	A549	lung:	n/a	chr6:30710267-30710280 chr6:30710688-30710697
32	MXI1	chr6:30709693-30711704	Hela-S3	cervix:	n/a	n/a
33	PBX3	chr6:30709824-30711034	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr6:30709500-30712522	GM18526	blood:	n/a	n/a
35	TCF7L2	chr6:30709572-30711603	Hela-S3	cervix:	n/a	chr6:30710204-30710213
36	POLR2A	chr6:30709207-30712588	HepG2	liver:	n/a	n/a
37	POU2F2	chr6:30709538-30711385	GM12891	blood:	n/a	n/a
38	MAX	chr6:30709328-30712883	HCT-116	colon:	n/a	chr6:30710671-30710680
39	EP300	chr6:30709752-30711160	A549	lung:	n/a	n/a
40	CHD1	chr6:30707429-30712681	IMR90	lung:	n/a	chr6:30710901-30710911 chr6:30710526-30710536
41	POLR2A	chr6:30709147-30712541	GM12892	blood:	n/a	n/a
42	STAT3	chr6:30709768-30710982	MCF10A-Er-Src	breast:	n/a	chr6:30710183-30710195
43	POLR2A	chr6:30709207-30712681	HCT-116	colon:	n/a	n/a
44	POLR2A	chr6:30709445-30712576	GM12891	blood:	n/a	n/a
45	CTCF	chr6:30709800-30709950	AG09319	gingival:	n/a	n/a
46	POLR2A	chr6:30707359-30712662	Hela-S3	cervix:	n/a	n/a
47	ZMIZ1	chr6:30709809-30712595	K562	blood:	n/a	n/a
48	TEAD4	chr6:30709194-30712744	K562	blood:	n/a	n/a
49	ELF1	chr6:30709282-30712770	HCT-116	colon:	n/a	n/a
50	RCOR1	chr6:30709830-30711185	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30709803-30709853	AG09319	gingival:	n/a
2	chr6:30709803-30709853	HPAEpiC	pulmonary alveolar:	n/a
3	chr6:30709803-30709853	SKMC	muscle:	n/a
4	chr6:30709803-30709853	SK-N-SH_RA	brain:	n/a
5	chr6:30709803-30709853	Hela-S3	cervix:	n/a
6	chr6:30709803-30709853	HCF	heart:	n/a
7	chr6:30709803-30709853	BJ	skin:	n/a
8	chr6:30709803-30709853	NB4	blood:	n/a
9	chr6:30709803-30709853	PANC-1	pancreas:	n/a
10	chr6:30709803-30709853	HMEC	breast:	n/a
11	chr6:30709803-30709853	PFSK-1	brain:	n/a
12	chr6:30709803-30709853	SK-N-MC	brain:	n/a
13	chr6:30709803-30709853	Hepatocyte	liver:	n/a
14	chr6:30709803-30709853	RPTEC	kidney:	n/a
15	chr6:30709803-30709853	K562	blood:	n/a
16	chr6:30709803-30709853	HRCEpiC	kidney:	n/a
17	chr6:30709803-30709853	HEEpiC	esophagus:	n/a
18	chr6:30709803-30709853	PrEC	prostate:	n/a
19	chr6:30709803-30709853	T-47D	breast:	n/a
20	chr6:30709803-30709853	ECC-1	luminal epithelium:	n/a
21	chr6:30709803-30709853	MCF-7	breast:	n/a
22	chr6:30709803-30709853	U87	brain:	n/a
23	chr6:30709803-30709853	AoSMC	blood vessel:	n/a
24	chr6:30709803-30709853	GM06990	blood:	n/a
25	chr6:30709803-30709853	HIPEpiC	eye:	n/a
26	chr6:30709803-30709853	CMK	blood:	n/a
27	chr6:30709803-30709853	GM12892	blood:	n/a
28	chr6:30709803-30709853	BE2_C	brain:	n/a
29	chr6:30709803-30709853	AG04449	skin:	fetal
30	chr6:30709803-30709853	SAEC	small airway:	n/a
31	chr6:30709803-30709853	ProgFib	skin:	n/a
32	chr6:30709803-30709853	HepG2	liver:	n/a
33	chr6:30709803-30709853	HCPEpiC	choroid plexus:	n/a
34	chr6:30709803-30709853	SK-N-SH	brain:	n/a
35	chr6:30709803-30709853	HL-60	blood:	n/a
36	chr6:30709803-30709853	NHBE	bronchial:	n/a
37	chr6:30709803-30709853	Jurkat	blood:	n/a
38	chr6:30709803-30709853	A549	lung:	n/a
39	chr6:30709803-30709853	HCT-116	colon:	n/a
40	chr6:30709803-30709853	IMR90	lung:	fetal
41	chr6:30709803-30709853	GM12878	blood:	n/a
42	chr6:30709803-30709853	HCM	heart:	n/a
43	chr6:30709803-30709853	Caco-2	colon:	n/a
44	chr6:30709803-30709853	AG04450	lung:	fetal
45	chr6:30709803-30709853	AG10803	skin:	n/a
46	chr6:30709803-30709853	NT2-D1	testis:	n/a
47	chr6:30709803-30709853	HRE	kidney:	n/a
48	chr6:30709803-30709853	HRPEpiC	eye:	n/a
49	chr6:30709803-30709853	NHDF-neo	bronchial:	n/a
50	chr6:30709803-30709853	HAEpiC	amniotic membrane:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30523845..30525398-chr6:30708449..30710069,2	MCF-7	breast:
2	chr6:30707945..30712505-chr6:30840794..30847673,9	K562	blood:
3	chr6:30707658..30710015-chr8:144677120..144679649,2	MCF-7	breast:
4	chr1:117451768..117453895-chr6:30707960..30710700,2	MCF-7	breast:
5	chr6:30709662..30710325-chr6:108881667..108882432,2	Hela-S3	cervix:
6	chr2:32581282..32582339-chr6:30709753..30710619,3	Hela-S3	cervix:
7	chr6:30581322..30587794-chr6:30705649..30714068,32	K562	blood:
8	chr6:30703666..30722133-chr6:30776009..30801352,184	MCF-7	breast:
9	chr12:6643028..6643863-chr6:30709743..30710630,2	Hela-S3	cervix:
10	chr6:30537817..30539494-chr6:30709502..30712304,2	K562	blood:
11	chr6:30639079..30642784-chr6:30705636..30712325,12	MCF-7	breast:
12	chr17:56030673..56033156-chr6:30709392..30711627,2	MCF-7	breast:
13	chr3:170587537..170588121-chr6:30709146..30709960,2	Hela-S3	cervix:
14	chr20:57556004..57557589-chr6:30709724..30711628,2	MCF-7	breast:
15	chr6:30707481..30713943-chr6:30872979..30880006,10	MCF-7	breast:
16	chr6:30614009..30615526-chr6:30709280..30711034,2	MCF-7	breast:
17	chr6:30709387..30712006-chr6:30881214..30883426,2	K562	blood:
18	chr11:118788904..118790575-chr6:30707843..30710033,2	MCF-7	breast:
19	chr6:30578948..30585851-chr6:30707403..30713755,14	MCF-7	breast:
20	chr6:30705171..30717521-chr6:30843972..30856100,74	MCF-7	breast:
21	chr1:145381364..145383003-chr6:30708944..30710900,2	MCF-7	breast:
22	chr6:30709658..30711296-chr6:30861145..30862930,2	MCF-7	breast:
23	chr6:30709801..30712369-chr9:116163469..116165342,2	MCF-7	breast:
24	chr6:30580645..30587403-chr6:30708153..30714600,16	MCF-7	breast:
25	chr11:82996745..82997289-chr6:30709394..30710375,2	Hela-S3	cervix:
26	chr6:30704403..30722478-chr6:30842859..30858629,100	MCF-7	breast:
27	chr11:62495454..62497939-chr6:30709047..30710768,2	MCF-7	breast:
28	chr6:30709669..30712213-chr6:30880810..30882538,2	MCF-7	breast:
29	chr6:30703055..30723531-chr6:30783853..30800217,151	MCF-7	breast:
30	chr6:30709563..30710317-chr8:91657123..91658008,2	Hela-S3	cervix:
31	chr17:57918223..57923763-chr6:30707801..30713436,10	MCF-7	breast:
32	chr6:30594160..30596394-chr6:30709286..30711112,2	MCF-7	breast:
33	chr19:59084038..59084620-chr6:30709785..30710614,2	Hela-S3	cervix:
34	chr6:30537121..30539529-chr6:30708411..30710426,2	MCF-7	breast:
35	chr6:30708700..30710764-chr6:30734085..30735975,2	K562	blood:
36	chr15:60687645..60690491-chr6:30708468..30710482,2	MCF-7	breast:
37	chr17:57922134..57925818-chr6:30708673..30712845,6	MCF-7	breast:
38	chr6:30709068..30709954-chr7:100026485..100027413,2	Hela-S3	cervix:
39	chr22:19418220..19420247-chr6:30709799..30711919,2	MCF-7	breast:
40	chr6:30707880..30713865-chr6:30880456..30883497,7	MCF-7	breast:
41	chr15:65596039..65597563-chr6:30709238..30711608,2	MCF-7	breast:
42	chr14:81685583..81687779-chr6:30708570..30711390,2	MCF-7	breast:
43	chr6:30651552..30657864-chr6:30708721..30713716,15	MCF-7	breast:

No data

Variant related genes	Relation type
FLOT1	TF binding region
ENSG00000272273	TF binding region
FLOT1	CpG island
ENSG00000272273	CpG island
ENSG00000200156	Chromatin interaction
ENSG00000146112	Chromatin interaction
ENSG00000185608	Chromatin interaction
ENSG00000264731	Chromatin interaction
ENSG00000137343	Chromatin interaction
ENSG00000182718	Chromatin interaction
ENSG00000222894	Chromatin interaction
ENSG00000104529	Chromatin interaction
ENSG00000165417	Chromatin interaction
ENSG00000180891	Chromatin interaction
ENSG00000204568	Chromatin interaction
ENSG00000101158	Chromatin interaction
ENSG00000204590	Chromatin interaction
ENSG00000272715	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000162222	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000180694	Chromatin interaction
ENSG00000111640	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000163584	Chromatin interaction
ENSG00000137411	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000204576	Chromatin interaction
ENSG00000118689	Chromatin interaction
ENSG00000137500	Chromatin interaction
ENSG00000099326	Chromatin interaction
ENSG00000100084	Chromatin interaction
ENSG00000186174	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000214894	Chromatin interaction
ENSG00000115760	Chromatin interaction
ENSG00000204574	Chromatin interaction
ENSG00000204580	Chromatin interaction
ENSG00000255234	Chromatin interaction
ENSG00000228022	Chromatin interaction
ENSG00000213780	Chromatin interaction
ENSG00000204560	Chromatin interaction
ENSG00000204569	Chromatin interaction
ENSG00000148218	Chromatin interaction
ENSG00000237775	Chromatin interaction
ENSG00000134247	Chromatin interaction
ENSG00000204564	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1049943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1061397	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1061424	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10947089	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1136719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12111310	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1264352	0.83[ASN][1000 genomes]
rs15297	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17189329	0.85[ASN][1000 genomes]
rs17195712	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28600807	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3094128	0.97[ASN][1000 genomes]
rs3130662	1.00[ASN][1000 genomes]
rs3909184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41270529	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58638768	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9968884	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9968888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9968913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9968960	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9969042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' 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	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	esv3430377	chr6:30443802-30814426	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS 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	967 gene(s)	inside rSNPs	diseases
5	nsv830626	chr6:30558064-30732905	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	406 gene(s)	inside rSNPs	diseases
6	esv2758041	chr6:30644693-30816319	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
7	esv2759413	chr6:30644693-30816319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
8	nsv970736	chr6:30692055-30710740	Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
9	nsv884100	chr6:30693816-30751326	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
10	nsv884101	chr6:30695920-30733121	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	163 gene(s)	inside rSNPs	diseases
11	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
12	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
13	nsv884102	chr6:30706013-30720567	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	158 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30708800-30710000	Flanking Active TSS	Hela-S3	cervix
2	chr6:30708800-30710200	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr6:30708800-30710200	Flanking Active TSS	Dnd41	blood
4	chr6:30708800-30710400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
5	chr6:30709000-30710000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr6:30709000-30710000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:30709000-30710000	Flanking Active TSS	Brain Anterior Caudate	brain
8	chr6:30709000-30710000	Flanking Active TSS	Duodenum Mucosa	Duodenum
9	chr6:30709000-30710200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
10	chr6:30709000-30710200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:30709000-30710200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr6:30709000-30710200	Flanking Active TSS	NH-A	brain
13	chr6:30709000-30710800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:30709000-30711200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:30709200-30710000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:30709200-30710000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
17	chr6:30709200-30710000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:30709200-30710000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:30709200-30710000	Flanking Active TSS	Liver	Liver
20	chr6:30709200-30710000	Flanking Active TSS	Brain Angular Gyrus	brain
21	chr6:30709200-30710000	Flanking Active TSS	Brain Substantia Nigra	brain
22	chr6:30709200-30710000	Flanking Active TSS	Colonic Mucosa	Colon
23	chr6:30709200-30710000	Flanking Active TSS	Colon Smooth Muscle	Colon
24	chr6:30709200-30710000	Flanking Active TSS	Fetal Brain Male	brain
25	chr6:30709200-30710000	Flanking Active TSS	Fetal Brain Female	brain
26	chr6:30709200-30710000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
27	chr6:30709200-30710000	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr6:30709200-30710000	Transcr. at gene 5' and 3'	HSMMtube	muscle
29	chr6:30709200-30710200	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr6:30709200-30710200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr6:30709200-30710200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr6:30709200-30710200	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
33	chr6:30709200-30710800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr6:30709200-30712600	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr6:30709200-30712600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:30709200-30712600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr6:30709200-30712600	Active TSS	HSMM	muscle
38	chr6:30709400-30710000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
39	chr6:30709400-30710000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:30709400-30710000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr6:30709400-30710000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr6:30709400-30710000	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr6:30709400-30710000	Flanking Active TSS	Brain Cingulate Gyrus	brain
44	chr6:30709400-30710000	Flanking Active TSS	Brain Germinal Matrix	brain
45	chr6:30709400-30710000	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr6:30709400-30710000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr6:30709400-30710000	Flanking Active TSS	Esophagus	oesophagus
48	chr6:30709400-30710000	Flanking Active TSS	Placenta	Placenta
49	chr6:30709400-30710000	Flanking Active TSS	Psoas Muscle	Psoas
50	chr6:30709400-30710000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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