Variant report

Variant	rs17201459
Chromosome Location	chr6:31926339-31926340
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31926315-31927314	GM12892	blood:	n/a	n/a
2	POLR2A	chr6:31926273-31927396	HUVEC	blood vessel:	n/a	n/a
3	SP4	chr6:31926330-31927077	H1-hESC	embryonic stem cell:	n/a	chr6:31926897-31926908
4	MAX	chr6:31926325-31927293	A549	lung:	n/a	n/a
5	ATF1	chr6:31926331-31927215	K562	blood:	n/a	n/a
6	GABPA	chr6:31926167-31927372	A549	lung:	n/a	n/a
7	POLR2A	chr6:31926218-31927259	MCF-7	breast:	n/a	n/a
8	MAX	chr6:31926287-31927262	NB4	blood:	n/a	n/a
9	CREB1	chr6:31926122-31927508	HepG2	liver:	n/a	n/a
10	YY1	chr6:31926331-31927255	HepG2	liver:	n/a	chr6:31926996-31927007
11	CREB1	chr6:31926206-31927349	GM12878	blood:	n/a	n/a
12	STAT5A	chr6:31926186-31927457	GM12878	blood:	n/a	chr6:31926997-31927009
13	ELF1	chr6:31926307-31927548	HCT-116	colon:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
14	CREB1	chr6:31926068-31927469	HepG2	liver:	n/a	n/a
15	SIN3A	chr6:31926296-31927154	GM12878	blood:	n/a	n/a
16	GABPA	chr6:31926124-31927388	SK-N-SH	brain:	n/a	n/a
17	NR2F2	chr6:31926331-31927666	K562	blood:	n/a	chr6:31927054-31927069 chr6:31927036-31927051 chr6:31927057-31927072
18	MXI1	chr6:31926047-31927579	SK-N-SH	brain:	n/a	n/a
19	MBD4	chr6:31926296-31927438	HepG2	liver:	n/a	n/a
20	TCF12	chr6:31926336-31927338	ECC-1	luminal epithelium:	n/a	n/a
21	GABPA	chr6:31926139-31927411	K562	blood:	n/a	n/a
22	TRIM28	chr6:31926327-31927312	K562	blood:	n/a	n/a
23	CREB1	chr6:31926306-31927216	ECC-1	luminal epithelium:	n/a	n/a
24	REST	chr6:31926118-31927391	H1-neurons	neurons:	n/a	chr6:31926851-31926864
25	SIN3AK20	chr6:31926198-31927189	SK-N-SH	brain:	n/a	n/a
26	SIN3AK20	chr6:31926094-31927214	K562	blood:	n/a	n/a
27	POLR2A	chr6:31925933-31927989	HepG2	liver:	n/a	n/a
28	MAZ	chr6:31926295-31927255	HepG2	liver:	n/a	n/a
29	POLR2A	chr6:31926327-31927207	SK-N-SH	brain:	n/a	n/a
30	SP1	chr6:31926259-31927447	HCT-116	colon:	n/a	chr6:31926996-31927005 chr6:31926995-31927007 chr6:31926897-31926908 chr6:31926992-31927006
31	HCFC1	chr6:31925525-31927640	Hela-S3	cervix:	n/a	n/a
32	ELF1	chr6:31926306-31927206	GM12878	blood:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
33	ATF3	chr6:31926263-31927384	K562	blood:	n/a	n/a
34	MAZ	chr6:31926085-31928360	IMR90	lung:	n/a	n/a
35	MYBL2	chr6:31926125-31927632	HepG2	liver:	n/a	n/a
36	MYC	chr6:31926219-31927262	K562	blood:	n/a	n/a
37	ELF1	chr6:31926230-31927520	MCF-7	breast:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
38	STAT5A	chr6:31926319-31927280	K562	blood:	n/a	chr6:31926997-31927009
39	JUN	chr6:31925824-31927905	K562	blood:	n/a	n/a
40	POLR2A	chr6:31926309-31927410	PFSK-1	brain:	n/a	n/a
41	MAX	chr6:31926155-31927242	ECC-1	luminal epithelium:	n/a	n/a
42	MAX	chr6:31926293-31927122	Hela-S3	cervix:	n/a	n/a
43	GABPA	chr6:31926236-31927369	SK-N-SH	brain:	n/a	n/a
44	ELF1	chr6:31926195-31927567	HCT-116	colon:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876
45	MYBL2	chr6:31926266-31927460	HepG2	liver:	n/a	n/a
46	MXI1	chr6:31926329-31927173	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr6:31926316-31926361	MCF-7	breast:	n/a	n/a
48	REST	chr6:31926289-31926508	H1-hESC	embryonic stem cell:	n/a	n/a
49	HDAC2	chr6:31926216-31927171	K562	blood:	n/a	n/a
50	ELF1	chr6:31926320-31927470	HepG2	liver:	n/a	chr6:31926932-31926945 chr6:31926864-31926877 chr6:31926867-31926876

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31926290-31926340	AG10803	skin:	n/a
2	chr6:31926290-31926340	A549	lung:	n/a
3	chr6:31926290-31926340	ovcar-3	ovarian:	n/a
4	chr6:31926290-31926340	HCM	heart:	n/a
5	chr6:31926290-31926340	NHDF-neo	bronchial:	n/a
6	chr6:31926290-31926340	AoSMC	blood vessel:	n/a
7	chr6:31926290-31926340	PrEC	prostate:	n/a
8	chr6:31926290-31926340	SK-N-MC	brain:	n/a
9	chr6:31926290-31926340	AG09319	gingival:	n/a
10	chr6:31926290-31926340	ProgFib	skin:	n/a
11	chr6:31926290-31926340	SKMC	muscle:	n/a
12	chr6:31926290-31926340	NB4	blood:	n/a
13	chr6:31926290-31926340	SAEC	small airway:	n/a
14	chr6:31926290-31926340	NH-A	brain:	n/a
15	chr6:31926290-31926340	GM12891	blood:	n/a
16	chr6:31926290-31926340	MCF-7	breast:	n/a
17	chr6:31926290-31926340	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:31926290-31926340	AG09309	skin:	n/a
19	chr6:31926290-31926340	Hepatocyte	liver:	n/a
20	chr6:31926290-31926340	HNPCEpiC	eye:	n/a
21	chr6:31926290-31926340	SK-N-SH	brain:	n/a
22	chr6:31926290-31926340	BE2_C	brain:	n/a
23	chr6:31926290-31926340	HIPEpiC	eye:	n/a
24	chr6:31926290-31926340	K562	blood:	n/a
25	chr6:31926290-31926340	T-47D	breast:	n/a
26	chr6:31926290-31926340	GM12892	blood:	n/a
27	chr6:31926290-31926340	HCT-116	colon:	n/a
28	chr6:31926290-31926340	Hela-S3	cervix:	n/a
29	chr6:31926290-31926340	HRE	kidney:	n/a
30	chr6:31926290-31926340	NHBE	bronchial:	n/a
31	chr6:31926290-31926340	HCPEpiC	choroid plexus:	n/a
32	chr6:31926290-31926340	CMK	blood:	n/a
33	chr6:31926290-31926340	IMR90	lung:	fetal
34	chr6:31926290-31926340	LNCaP	prostate:	n/a
35	chr6:31926290-31926340	PANC-1	pancreas:	n/a
36	chr6:31926290-31926340	HAEpiC	amniotic membrane:	n/a
37	chr6:31926290-31926340	HUVEC	blood vessel:	n/a
38	chr6:31926290-31926340	BJ	skin:	n/a
39	chr6:31926290-31926340	HEEpiC	esophagus:	n/a
40	chr6:31926290-31926340	GM19239	blood:	n/a
41	chr6:31926290-31926340	U87	brain:	n/a
42	chr6:31926290-31926340	AG04449	skin:	fetal
43	chr6:31926290-31926340	GM06990	blood:	n/a
44	chr6:31926290-31926340	ECC-1	luminal epithelium:	n/a
45	chr6:31926290-31926340	HMEC	breast:	n/a
46	chr6:31926290-31926340	Caco-2	colon:	n/a
47	chr6:31926290-31926340	HL-60	blood:	n/a
48	chr6:31926290-31926340	HEK293	kidney:	embryo
49	chr6:31926290-31926340	PFSK-1	brain:	n/a
50	chr6:31926290-31926340	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:31781796..31783894-chr6:31925428..31927086,2	K562	blood:
2	chr6:31634033..31636196-chr6:31925448..31927170,2	K562	blood:
3	chr6:31844767..31847605-chr6:31925658..31928567,2	MCF-7	breast:
4	chr6:31862879..31872535-chr6:31911667..31928766,47	MCF-7	breast:
5	chr6:31830490..31833199-chr6:31923802..31927860,4	MCF-7	breast:
6	chr6:31864040..31872511-chr6:31917614..31930102,27	MCF-7	breast:
7	chr6:31864712..31866806-chr6:31924793..31927734,3	K562	blood:
8	chr6:31894560..31897888-chr6:31924484..31928410,3	K562	blood:
9	chr6:31829193..31831687-chr6:31925120..31927788,2	MCF-7	breast:
10	chr6:31799457..31804164-chr6:31924693..31928301,4	K562	blood:
11	chr6:31632061..31634821-chr6:31925160..31927798,3	MCF-7	breast:
12	chr6:31867895..31873109-chr6:31925613..31930389,7	K562	blood:
13	chr6:31800973..31803192-chr6:31924804..31927036,2	MCF-7	breast:
14	chr6:31845134..31847319-chr6:31924612..31926592,2	MCF-7	breast:
15	chr6:31925015..31926680-chr6:32161987..32163956,2	K562	blood:
16	chr6:31894560..31897888-chr6:31924484..31926934,4	K562	blood:

No data

Variant related genes	Relation type
MIR1236	TF binding region
SKIV2L	TF binding region
NELFE	TF binding region
SKIV2L	CpG island
NELFE	CpG island
MIR1236	CpG island
ENSG00000263020	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000244255	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000204366	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs59402363	1.00[AMR][1000 genomes]
rs59979480	1.00[AMR][1000 genomes]
rs73729004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73729005	1.00[AMR][1000 genomes]
rs9461723	1.00[AMR][1000 genomes]
rs9469037	1.00[AMR][1000 genomes]
rs9469039	1.00[AMR][1000 genomes]
rs9469048	1.00[AMR][1000 genomes]
rs9469078	1.00[AMR][1000 genomes]
rs9501163	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
11	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' 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	197 gene(s)	inside rSNPs	diseases
12	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
13	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
14	nsv601961	chr6:31868322-32484368	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
15	nsv427751	chr6:31871512-32092843	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
16	nsv428141	chr6:31871512-32092843	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
17	esv2758043	chr6:31871512-32209113	Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	esv2759415	chr6:31871512-32209113	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
19	nsv830628	chr6:31887554-31947600	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
20	nsv933250	chr6:31905060-32008005	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
21	nsv934279	chr6:31905060-32013902	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv884512	chr6:31908470-31933161	Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
23	nsv884513	chr6:31922575-32066025	Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
24	nsv884514	chr6:31923052-31958960	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
25	nsv932869	chr6:31924496-32013902	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
26	nsv933913	chr6:31924682-32009282	Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
27	nsv284	chr6:31925739-31996721	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
28	nsv5247	chr6:31925739-32023216	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 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	chr6:31925200-31926400	Flanking Active TSS	Dnd41	blood
2	chr6:31925400-31926400	Flanking Active TSS	GM12878-XiMat	blood
3	chr6:31925600-31926400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:31925600-31926400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:31925600-31926400	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr6:31925600-31926400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr6:31925600-31926400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:31925600-31926400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:31925600-31926400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr6:31925600-31926600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr6:31925600-31927800	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr6:31925800-31926400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr6:31925800-31926400	Flanking Active TSS	Primary T cells from cord blood	blood
14	chr6:31925800-31926400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
15	chr6:31925800-31926400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr6:31925800-31926400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr6:31925800-31926400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
18	chr6:31925800-31926400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr6:31925800-31926400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:31925800-31926400	Flanking Active TSS	Brain Angular Gyrus	brain
21	chr6:31925800-31926400	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr6:31925800-31926400	Flanking Active TSS	Brain Germinal Matrix	brain
23	chr6:31925800-31926400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
24	chr6:31925800-31926400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr6:31925800-31926400	Flanking Active TSS	Colonic Mucosa	Colon
26	chr6:31925800-31926400	Flanking Active TSS	Duodenum Mucosa	Duodenum
27	chr6:31925800-31926400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr6:31925800-31926400	Flanking Active TSS	Fetal Brain Male	brain
29	chr6:31925800-31926400	Flanking Active TSS	Fetal Muscle Leg	muscle
30	chr6:31925800-31926400	Flanking Active TSS	Placenta	Placenta
31	chr6:31925800-31926400	Flanking Active TSS	Fetal Stomach	stomach
32	chr6:31925800-31926400	Flanking Active TSS	Fetal Thymus	thymus
33	chr6:31925800-31926400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
34	chr6:31925800-31926400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr6:31925800-31926400	Flanking Active TSS	HUVEC	blood vessel
36	chr6:31925800-31926400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr6:31925800-31926600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr6:31925800-31926600	Flanking Active TSS	Primary B cells from cord blood	blood
39	chr6:31925800-31926600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr6:31925800-31926600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr6:31925800-31926600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr6:31925800-31926600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:31925800-31926600	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr6:31925800-31926600	Flanking Active TSS	Liver	Liver
45	chr6:31925800-31926600	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr6:31925800-31926600	Flanking Active TSS	Thymus	Thymus
47	chr6:31925800-31927200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr6:31925800-31927200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:31925800-31927200	Active TSS	NHDF-Ad	bronchial
50	chr6:31925800-31927400	Active TSS	ES-I3 Cell Line	embryonic stem cell

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