Variant report

Variant	rs13194402
Chromosome Location	chr6:31707344-31707345
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31703182-31707401	HepG2	liver:	n/a	n/a
2	FOXM1	chr6:31707199-31708212	GM12878	blood:	n/a	n/a
3	ELF1	chr6:31707272-31708451	GM12878	blood:	n/a	n/a
4	HEY1	chr6:31706945-31707571	HepG2	liver:	n/a	n/a
5	E2F6	chr6:31707222-31708644	H1-hESC	embryonic stem cell:	n/a	chr6:31707584-31707596 chr6:31707852-31707859 chr6:31707851-31707859 chr6:31707851-31707860 chr6:31707852-31707859 chr6:31707849-31707860 chr6:31707852-31707859 chr6:31707849-31707863 chr6:31707848-31707860 chr6:31707743-31707752 chr6:31707768-31707777
6	ZBTB7A	chr6:31707137-31707618	HepG2	liver:	n/a	n/a
7	POLR2A	chr6:31705275-31708451	K562	blood:	n/a	n/a
8	TBP	chr6:31707049-31708037	HepG2	liver:	n/a	n/a
9	SP2	chr6:31707317-31707939	HepG2	liver:	n/a	n/a
10	POLR2A	chr6:31707217-31708475	SK-N-MC	brain:	n/a	n/a
11	HEY1	chr6:31706843-31708524	K562	blood:	n/a	n/a
12	RELA	chr6:31705651-31707748	GM18526	blood:	n/a	n/a
13	EP300	chr6:31705155-31708063	HepG2	liver:	n/a	chr6:31707141-31707149
14	STAT5A	chr6:31706862-31708411	K562	blood:	n/a	chr6:31708108-31708120 chr6:31707672-31707684
15	JUND	chr6:31707288-31708202	H1-hESC	embryonic stem cell:	n/a	chr6:31707528-31707537 chr6:31707631-31707640
16	POLR2A	chr6:31707280-31708135	MCF10A-Er-Src	breast:	n/a	n/a
17	MAFF	chr6:31707027-31707586	K562	blood:	n/a	n/a
18	NFIC	chr6:31706454-31708274	GM12878	blood:	n/a	n/a
19	CHD2	chr6:31706466-31708006	GM12878	blood:	n/a	n/a
20	HEY1	chr6:31700825-31708048	HepG2	liver:	n/a	n/a
21	GATA3	chr6:31707074-31708247	A549	lung:	n/a	chr6:31707881-31707898 chr6:31707395-31707405
22	POLR2A	chr6:31706852-31709097	PANC-1	pancreas:	n/a	n/a
23	ZC3H11A	chr6:31707007-31708304	K562	blood:	n/a	n/a
24	SIN3AK20	chr6:31707289-31708448	K562	blood:	n/a	n/a
25	TAF1	chr6:31707239-31708491	K562	blood:	n/a	n/a
26	MAFK	chr6:31707145-31707873	HepG2	liver:	n/a	n/a
27	FOXA1	chr6:31705175-31708069	HepG2	liver:	n/a	chr6:31706270-31706285
28	ZMIZ1	chr6:31705309-31708339	K562	blood:	n/a	n/a
29	MAX	chr6:31707126-31708370	SK-N-SH	brain:	n/a	chr6:31707734-31707744
30	POLR2A	chr6:31707339-31708433	GM12892	blood:	n/a	n/a
31	FOXA2	chr6:31706854-31707965	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:31707254-31708193	GM12878	blood:	n/a	n/a
33	MBD4	chr6:31705115-31708186	HepG2	liver:	n/a	n/a
34	POLR2A	chr6:31707155-31708615	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr6:31707331-31708517	ECC-1	luminal epithelium:	n/a	n/a
36	SP1	chr6:31707150-31708235	HCT-116	colon:	n/a	chr6:31707734-31707744 chr6:31707734-31707743 chr6:31707730-31707744 chr6:31707735-31707744 chr6:31707733-31707745 chr6:31707580-31707594 chr6:31707609-31707618 chr6:31707733-31707745 chr6:31707628-31707649 chr6:31708099-31708109
37	TEAD4	chr6:31705115-31708474	K562	blood:	n/a	n/a
38	MYC	chr6:31707063-31708612	NB4	blood:	n/a	chr6:31707734-31707744
39	RELA	chr6:31705616-31708216	GM19193	blood:	n/a	n/a
40	YY1	chr6:31707296-31708682	GM12878	blood:	n/a	chr6:31708110-31708121
41	TCF12	chr6:31707075-31707670	HepG2	liver:	n/a	n/a
42	MAZ	chr6:31705267-31708428	K562	blood:	n/a	chr6:31705423-31705432 chr6:31707734-31707744
43	CHD2	chr6:31707325-31708327	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr6:31707115-31707835	HepG2	liver:	n/a	chr6:31707528-31707537 chr6:31707631-31707640
45	POLR2A	chr6:31707286-31708408	HCT-116	colon:	n/a	n/a
46	HNF4G	chr6:31707052-31707997	HepG2	liver:	n/a	n/a
47	POLR2A	chr6:31707013-31708479	GM18526	blood:	n/a	n/a
48	SP1	chr6:31705167-31708177	A549	lung:	n/a	chr6:31706876-31706885 chr6:31707734-31707744 chr6:31707734-31707743 chr6:31707730-31707744 chr6:31707735-31707744 chr6:31706098-31706107 chr6:31707733-31707745 chr6:31705835-31705848 chr6:31705486-31705496 chr6:31707580-31707594 chr6:31707609-31707618 chr6:31705486-31705495 chr6:31706875-31706885 chr6:31707733-31707745 chr6:31707628-31707649 chr6:31706755-31706769 chr6:31708099-31708109
49	JUND	chr6:31705274-31708376	K562	blood:	n/a	chr6:31707528-31707537 chr6:31707631-31707640
50	RCOR1	chr6:31707045-31707938	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31707301-31707351	SK-N-SH	brain:	n/a
2	chr6:31707301-31707351	AG04450	lung:	fetal
3	chr6:31707301-31707351	Caco-2	colon:	n/a
4	chr6:31707301-31707351	NHDF-neo	bronchial:	n/a
5	chr6:31707301-31707351	HRPEpiC	eye:	n/a
6	chr6:31707301-31707351	GM12892	blood:	n/a
7	chr6:31707301-31707351	PrEC	prostate:	n/a
8	chr6:31707301-31707351	K562	blood:	n/a
9	chr6:31707301-31707351	GM12878	blood:	n/a
10	chr6:31707301-31707351	T-47D	breast:	n/a
11	chr6:31707301-31707351	SKMC	muscle:	n/a
12	chr6:31707301-31707351	NT2-D1	testis:	n/a
13	chr6:31707301-31707351	HIPEpiC	eye:	n/a
14	chr6:31707301-31707351	HL-60	blood:	n/a
15	chr6:31707301-31707351	AG04449	skin:	fetal
16	chr6:31707301-31707351	PANC-1	pancreas:	n/a
17	chr6:31707301-31707351	HCPEpiC	choroid plexus:	n/a
18	chr6:31707301-31707351	HNPCEpiC	eye:	n/a
19	chr6:31707301-31707351	BE2_C	brain:	n/a
20	chr6:31707301-31707351	SAEC	small airway:	n/a
21	chr6:31707301-31707351	HCF	heart:	n/a
22	chr6:31707301-31707351	HRCEpiC	kidney:	n/a
23	chr6:31707301-31707351	CMK	blood:	n/a
24	chr6:31707301-31707351	A549	lung:	n/a
25	chr6:31707301-31707351	MCF-7	breast:	n/a
26	chr6:31707301-31707351	NH-A	brain:	n/a
27	chr6:31707301-31707351	NHBE	bronchial:	n/a
28	chr6:31707301-31707351	H1-hESC	embryonic stem cell:	embryo
29	chr6:31707301-31707351	HUVEC	blood vessel:	n/a
30	chr6:31707301-31707351	ovcar-3	ovarian:	n/a
31	chr6:31707301-31707351	PFSK-1	brain:	n/a
32	chr6:31707301-31707351	AG10803	skin:	n/a
33	chr6:31707301-31707351	Jurkat	blood:	n/a
34	chr6:31707301-31707351	SK-N-MC	brain:	n/a
35	chr6:31707301-31707351	IMR90	lung:	fetal
36	chr6:31707301-31707351	HRE	kidney:	n/a
37	chr6:31707301-31707351	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:31707301-31707351	ProgFib	skin:	n/a
39	chr6:31707301-31707351	HCM	heart:	n/a
40	chr6:31707301-31707351	HEK293	kidney:	embryo
41	chr6:31707301-31707351	LNCaP	prostate:	n/a
42	chr6:31707301-31707351	SK-N-SH_RA	brain:	n/a
43	chr6:31707301-31707351	AG09309	skin:	n/a
44	chr6:31707301-31707351	AoSMC	blood vessel:	n/a
45	chr6:31707301-31707351	GM19239	blood:	n/a
46	chr6:31707301-31707351	HepG2	liver:	n/a
47	chr6:31707301-31707351	BJ	skin:	n/a
48	chr6:31707301-31707351	U87	brain:	n/a
49	chr6:31707301-31707351	MCF10A-Er-Src	breast:	n/a
50	chr6:31707301-31707351	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:31673061..31674649-chr6:31705236..31707365,2	MCF-7	breast:
2	chr6:31513726..31516111-chr6:31705969..31708009,2	MCF-7	breast:
3	chr11:62608594..62609131-chr6:31706624..31707363,2	Hela-S3	cervix:
4	chr6:31706534..31708652-chr6:31828813..31831366,2	K562	blood:
5	chr6:31704202..31707346-chr6:32935794..32939096,3	K562	blood:
6	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
7	chr6:31705886..31708099-chr6:31864785..31867152,2	K562	blood:
8	chr1:45285449..45286205-chr6:31707205..31707859,2	Hela-S3	cervix:
9	chr6:31705956..31708779-chr6:32940419..32942234,2	K562	blood:
10	chr6:31706414..31709644-chr6:31760309..31763318,4	MCF-7	breast:
11	chr6:31706404..31710413-chr6:31739544..31742193,3	MCF-7	breast:
12	chr6:31619534..31622102-chr6:31706429..31708950,2	MCF-7	breast:
13	chr6:31705740..31708202-chr6:31937563..31940759,3	K562	blood:
14	chr6:31706953..31708752-chr6:31729698..31731457,2	MCF-7	breast:
15	chr16:2517703..2518281-chr6:31706928..31707442,2	Hela-S3	cervix:
16	chr6:31513816..31516540-chr6:31705988..31708603,3	K562	blood:
17	chr6:31646441..31651407-chr6:31704606..31708985,8	MCF-7	breast:
18	chr6:31684407..31687044-chr6:31706148..31707920,2	MCF-7	breast:
19	chr6:31668441..31672326-chr6:31702683..31707609,7	MCF-7	breast:
20	chr6:31656167..31662607-chr6:31701760..31709122,7	MCF-7	breast:
21	chr6:31706634..31708801-chr6:31800658..31802483,2	MCF-7	breast:
22	chr6:31706679..31708956-chr6:31795250..31798080,2	MCF-7	breast:
23	chr6:31704899..31707815-chr6:31914437..31917102,2	MCF-7	breast:
24	chr6:31706580..31708960-chr6:31728802..31732177,3	MCF-7	breast:
25	chr6:31705460..31708202-chr6:31937853..31939865,2	K562	blood:
26	chr6:31632814..31634832-chr6:31706820..31709460,2	MCF-7	breast:

Variant related genes	Relation type
MSH5-SAPCD1	TF binding region
MSH5	TF binding region
CLIC1	TF binding region
MSH5-SAPCD1	CpG island
CLIC1	CpG island
MSH5	CpG island
ENSG00000204371	Chromatin interaction
ENSG00000266776	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000259895	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204420	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204388	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000228727	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000202444	Chromatin interaction
ENSG00000204424	Chromatin interaction
ENSG00000263756	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11552113	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13204983	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13211189	0.83[ASN][1000 genomes]
rs13211368	0.83[ASN][1000 genomes]
rs17200810	0.83[ASN][1000 genomes]
rs3093672	0.83[ASN][1000 genomes]
rs34038095	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34287387	1.00[ASN][1000 genomes]
rs34422607	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34451538	0.83[ASN][1000 genomes]
rs34568880	0.83[ASN][1000 genomes]
rs35012663	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35340190	0.83[ASN][1000 genomes]
rs35700586	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35963002	0.83[ASN][1000 genomes]
rs35969216	0.83[ASN][1000 genomes]
rs41267058	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41273252	0.83[ASN][1000 genomes]
rs4647191	0.83[ASN][1000 genomes]
rs71563354	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563359	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563361	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71563362	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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	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
12	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
13	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
14	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31702400-31708800	Flanking Active TSS	Primary hematopoietic stem cells	blood
2	chr6:31704200-31709000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:31704200-31709000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:31704400-31707400	Enhancers	Spleen	Spleen
5	chr6:31704400-31707400	Flanking Active TSS	Dnd41	blood
6	chr6:31704400-31707600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:31704400-31707600	Flanking Active TSS	Fetal Thymus	thymus
8	chr6:31704400-31708800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr6:31704400-31709000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr6:31704600-31707400	Weak transcription	Ovary	ovary
11	chr6:31704600-31707600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
12	chr6:31704600-31707600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr6:31704600-31707800	Enhancers	Placenta Amnion	Placenta Amnion
14	chr6:31704800-31707800	Weak transcription	Aorta	Aorta
15	chr6:31705000-31707400	Weak transcription	Right Atrium	heart
16	chr6:31705000-31707600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:31705000-31707600	Enhancers	Placenta	Placenta
18	chr6:31705200-31707400	Flanking Active TSS	K562	blood
19	chr6:31705400-31707400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:31705400-31707400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr6:31705400-31707400	Flanking Active TSS	Hela-S3	cervix
22	chr6:31705600-31707400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:31705600-31707400	Flanking Active TSS	NHEK	skin
24	chr6:31705600-31707800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:31706000-31707400	Enhancers	Fetal Heart	heart
26	chr6:31706200-31707400	Enhancers	Primary B cells from peripheral blood	blood
27	chr6:31706200-31707400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:31706200-31707400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr6:31706400-31707400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr6:31706400-31707600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:31706400-31707600	Weak transcription	Gastric	stomach
32	chr6:31706600-31707400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr6:31706600-31707400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:31706600-31707400	Enhancers	Esophagus	oesophagus
35	chr6:31706600-31707600	Weak transcription	Left Ventricle	heart
36	chr6:31706600-31707800	Weak transcription	Lung	lung
37	chr6:31706600-31708800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:31706600-31708800	Active TSS	A549	lung
39	chr6:31706800-31708800	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr6:31707000-31707400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:31707000-31707400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:31707000-31707400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:31707000-31707400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr6:31707000-31707400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr6:31707000-31707400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr6:31707000-31707400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr6:31707000-31707400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:31707000-31707400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:31707000-31707400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr6:31707000-31707400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain

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