Variant report

Variant	rs28381344
Chromosome Location	chr6:31707526-31707527
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:407)
CpG islands
(count:244)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXM1	chr6:31707199-31708212	GM12878	blood:	n/a	n/a
2	MYC	chr6:31707388-31708260	K562	blood:	n/a	chr6:31707734-31707744
3	POLR2A	chr6:31707362-31708488	GM10847	blood:	n/a	n/a
4	ELF1	chr6:31707272-31708451	GM12878	blood:	n/a	n/a
5	IRF3	chr6:31707462-31707831	GM12878	blood:	n/a	chr6:31707733-31707747
6	HEY1	chr6:31706945-31707571	HepG2	liver:	n/a	n/a
7	FOXP2	chr6:31707408-31707944	SK-N-MC	brain:	n/a	n/a
8	RFX5	chr6:31707410-31707844	GM12878	blood:	n/a	chr6:31707630-31707639 chr6:31707566-31707580
9	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
10	ZBTB7A	chr6:31707137-31707618	HepG2	liver:	n/a	n/a
11	POLR2A	chr6:31705275-31708451	K562	blood:	n/a	n/a
12	TBP	chr6:31707049-31708037	HepG2	liver:	n/a	n/a
13	SP2	chr6:31707317-31707939	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:31707217-31708475	SK-N-MC	brain:	n/a	n/a
15	MYC	chr6:31707398-31708064	H1-hESC	embryonic stem cell:	n/a	chr6:31707734-31707744
16	HEY1	chr6:31706843-31708524	K562	blood:	n/a	n/a
17	SP2	chr6:31707381-31707895	K562	blood:	n/a	n/a
18	RELA	chr6:31705651-31707748	GM18526	blood:	n/a	n/a
19	EP300	chr6:31705155-31708063	HepG2	liver:	n/a	chr6:31707141-31707149
20	TAF1	chr6:31707444-31708123	HepG2	liver:	n/a	n/a
21	STAT5A	chr6:31706862-31708411	K562	blood:	n/a	chr6:31708108-31708120 chr6:31707672-31707684
22	JUND	chr6:31707288-31708202	H1-hESC	embryonic stem cell:	n/a	chr6:31707528-31707537 chr6:31707631-31707640
23	POLR2A	chr6:31707280-31708135	MCF10A-Er-Src	breast:	n/a	n/a
24	MAFF	chr6:31707027-31707586	K562	blood:	n/a	n/a
25	NFIC	chr6:31706454-31708274	GM12878	blood:	n/a	n/a
26	POLR2A	chr6:31707453-31708731	MCF-7	breast:	n/a	n/a
27	CHD2	chr6:31706466-31708006	GM12878	blood:	n/a	n/a
28	HEY1	chr6:31700825-31708048	HepG2	liver:	n/a	n/a
29	GATA3	chr6:31707074-31708247	A549	lung:	n/a	chr6:31707881-31707898 chr6:31707395-31707405
30	YY1	chr6:31707512-31708511	H1-hESC	embryonic stem cell:	n/a	chr6:31708110-31708121
31	POLR2A	chr6:31706852-31709097	PANC-1	pancreas:	n/a	n/a
32	MYC	chr6:31707362-31708289	K562	blood:	n/a	chr6:31707734-31707744
33	ZC3H11A	chr6:31707007-31708304	K562	blood:	n/a	n/a
34	MXI1	chr6:31707387-31708084	Hela-S3	cervix:	n/a	n/a
35	TAF1	chr6:31707379-31708008	SK-N-SH	brain:	n/a	n/a
36	MYC	chr6:31707459-31707954	HepG2	liver:	n/a	chr6:31707734-31707744
37	SIN3AK20	chr6:31707289-31708448	K562	blood:	n/a	n/a
38	TAF1	chr6:31707239-31708491	K562	blood:	n/a	n/a
39	MAFK	chr6:31707145-31707873	HepG2	liver:	n/a	n/a
40	FOXA1	chr6:31705175-31708069	HepG2	liver:	n/a	chr6:31706270-31706285
41	ZMIZ1	chr6:31705309-31708339	K562	blood:	n/a	n/a
42	MAX	chr6:31707126-31708370	SK-N-SH	brain:	n/a	chr6:31707734-31707744
43	POLR2A	chr6:31707339-31708433	GM12892	blood:	n/a	n/a
44	FOXA2	chr6:31706854-31707965	HepG2	liver:	n/a	n/a
45	BHLHE40	chr6:31707254-31708193	GM12878	blood:	n/a	n/a
46	MBD4	chr6:31705115-31708186	HepG2	liver:	n/a	n/a
47	POLR2A	chr6:31707155-31708615	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr6:31707331-31708517	ECC-1	luminal epithelium:	n/a	n/a
49	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
50	TEAD4	chr6:31705115-31708474	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31707513-31707563	K562	blood:	n/a
2	chr6:31707490-31707540	SK-N-MC	brain:	n/a
3	chr6:31707511-31707561	PFSK-1	brain:	n/a
4	chr6:31707502-31707552	SK-N-SH	brain:	n/a
5	chr6:31707513-31707563	HCT-116	colon:	n/a
6	chr6:31707502-31707552	U87	brain:	n/a
7	chr6:31707490-31707540	BE2_C	brain:	n/a
8	chr6:31707511-31707561	ovcar-3	ovarian:	n/a
9	chr6:31707502-31707552	HRCEpiC	kidney:	n/a
10	chr6:31707513-31707563	NB4	blood:	n/a
11	chr6:31707502-31707552	HRPEpiC	eye:	n/a
12	chr6:31707490-31707540	ProgFib	skin:	n/a
13	chr6:31707511-31707561	HEEpiC	esophagus:	n/a
14	chr6:31707513-31707563	HRE	kidney:	n/a
15	chr6:31707513-31707563	HEEpiC	esophagus:	n/a
16	chr6:31707513-31707563	MCF-7	breast:	n/a
17	chr6:31707513-31707563	LNCaP	prostate:	n/a
18	chr6:31707502-31707552	GM06990	blood:	n/a
19	chr6:31707513-31707563	T-47D	breast:	n/a
20	chr6:31707490-31707540	U87	brain:	n/a
21	chr6:31707502-31707552	HRE	kidney:	n/a
22	chr6:31707513-31707563	BJ	skin:	n/a
23	chr6:31707490-31707540	Hela-S3	cervix:	n/a
24	chr6:31707511-31707561	SK-N-SH	brain:	n/a
25	chr6:31707511-31707561	HRE	kidney:	n/a
26	chr6:31707490-31707540	PrEC	prostate:	n/a
27	chr6:31707502-31707552	GM12891	blood:	n/a
28	chr6:31707513-31707563	HAEpiC	amniotic membrane:	n/a
29	chr6:31707511-31707561	AG09309	skin:	n/a
30	chr6:31707513-31707563	HEK293	kidney:	embryo
31	chr6:31707511-31707561	HCT-116	colon:	n/a
32	chr6:31707502-31707552	PFSK-1	brain:	n/a
33	chr6:31707490-31707540	SK-N-SH	brain:	n/a
34	chr6:31707490-31707540	NHDF-neo	bronchial:	n/a
35	chr6:31707511-31707561	H1-hESC	embryonic stem cell:	embryo
36	chr6:31707511-31707561	HRPEpiC	eye:	n/a
37	chr6:31707490-31707540	GM12891	blood:	n/a
38	chr6:31707513-31707563	MCF10A-Er-Src	breast:	n/a
39	chr6:31707513-31707563	HNPCEpiC	eye:	n/a
40	chr6:31707502-31707552	AG04449	skin:	fetal
41	chr6:31707490-31707540	HCF	heart:	n/a
42	chr6:31707490-31707540	SAEC	small airway:	n/a
43	chr6:31707513-31707563	HIPEpiC	eye:	n/a
44	chr6:31707511-31707561	Jurkat	blood:	n/a
45	chr6:31707511-31707561	GM12891	blood:	n/a
46	chr6:31707502-31707552	AG09309	skin:	n/a
47	chr6:31707502-31707552	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:31707502-31707552	MCF-7	breast:	n/a
49	chr6:31707511-31707561	U87	brain:	n/a
50	chr6:31707513-31707563	HMEC	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31513726..31516111-chr6:31705969..31708009,2	MCF-7	breast:
2	chr6:31706534..31708652-chr6:31828813..31831366,2	K562	blood:
3	chr6:31707439..31709705-chr6:31719652..31722031,2	MCF-7	breast:
4	chr6:31706755..31708433-chr6:31830637..31832576,2	K562	blood:
5	chr6:31705886..31708099-chr6:31864785..31867152,2	K562	blood:
6	chr1:45285449..45286205-chr6:31707205..31707859,2	Hela-S3	cervix:
7	chr6:31705956..31708779-chr6:32940419..32942234,2	K562	blood:
8	chr6:31706414..31709644-chr6:31760309..31763318,4	MCF-7	breast:
9	chr6:31706404..31710413-chr6:31739544..31742193,3	MCF-7	breast:
10	chr6:31619534..31622102-chr6:31706429..31708950,2	MCF-7	breast:
11	chr6:31705740..31708202-chr6:31937563..31940759,3	K562	blood:
12	chr6:31706953..31708752-chr6:31729698..31731457,2	MCF-7	breast:
13	chr6:31513816..31516540-chr6:31705988..31708603,3	K562	blood:
14	chr6:31646441..31651407-chr6:31704606..31708985,8	MCF-7	breast:
15	chr6:31684407..31687044-chr6:31706148..31707920,2	MCF-7	breast:
16	chr6:31668441..31672326-chr6:31702683..31707609,7	MCF-7	breast:
17	chr6:31656167..31662607-chr6:31701760..31709122,7	MCF-7	breast:
18	chr6:31706634..31708801-chr6:31800658..31802483,2	MCF-7	breast:
19	chr6:31706679..31708956-chr6:31795250..31798080,2	MCF-7	breast:
20	chr6:31704899..31707815-chr6:31914437..31917102,2	MCF-7	breast:
21	chr6:31706580..31708960-chr6:31728802..31732177,3	MCF-7	breast:
22	chr6:31705460..31708202-chr6:31937853..31939865,2	K562	blood:
23	chr6:31632814..31634832-chr6:31706820..31709460,2	MCF-7	breast:

No data

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

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs17207190	0.83[AMR][1000 genomes]
rs2516474	0.83[AMR][1000 genomes]
rs28732141	0.83[AMR][1000 genomes]
rs28732142	0.83[AMR][1000 genomes]
rs28732143	0.83[AMR][1000 genomes]
rs28732144	0.83[AMR][1000 genomes]
rs28732145	1.00[AMR][1000 genomes]
rs28732152	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs28732153	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28732155	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28732156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28732159	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28732160	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28732162	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28732164	1.00[AMR][1000 genomes]
rs28732165	1.00[AMR][1000 genomes]
rs28732166	1.00[AMR][1000 genomes]
rs28895015	0.83[AMR][1000 genomes]
rs28895017	1.00[AMR][1000 genomes]
rs3093726	0.83[AMR][1000 genomes]
rs3093727	0.83[AMR][1000 genomes]
rs35664695	1.00[AMR][1000 genomes]
rs41293911	0.83[AMR][1000 genomes]
rs41293915	0.83[AMR][1000 genomes]
rs41293919	0.83[AMR][1000 genomes]
rs41293923	0.83[AMR][1000 genomes]
rs41315808	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41315812	1.00[AMR][1000 genomes]
rs7757383	0.83[AMR][1000 genomes]
rs9368699	1.00[AFR][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	chr6:31704400-31707600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:31704400-31707600	Flanking Active TSS	Fetal Thymus	thymus
6	chr6:31704400-31708800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr6:31704400-31709000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr6:31704600-31707600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
9	chr6:31704600-31707600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr6:31704600-31707800	Enhancers	Placenta Amnion	Placenta Amnion
11	chr6:31704800-31707800	Weak transcription	Aorta	Aorta
12	chr6:31705000-31707600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:31705000-31707600	Enhancers	Placenta	Placenta
14	chr6:31705600-31707800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:31706400-31707600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr6:31706400-31707600	Weak transcription	Gastric	stomach
17	chr6:31706600-31707600	Weak transcription	Left Ventricle	heart
18	chr6:31706600-31707800	Weak transcription	Lung	lung
19	chr6:31706600-31708800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:31706600-31708800	Active TSS	A549	lung
21	chr6:31706800-31708800	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr6:31707000-31707600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
23	chr6:31707000-31707600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr6:31707000-31707600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
25	chr6:31707000-31707600	Flanking Active TSS	Fetal Intestine Large	intestine
26	chr6:31707000-31707600	Flanking Active TSS	Fetal Intestine Small	intestine
27	chr6:31707000-31707600	Flanking Active TSS	Fetal Stomach	stomach
28	chr6:31707000-31707600	Flanking Active TSS	Thymus	Thymus
29	chr6:31707000-31707600	Flanking Active TSS	HUVEC	blood vessel
30	chr6:31707000-31707800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:31707000-31708400	Flanking Active TSS	Liver	Liver
32	chr6:31707000-31708400	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr6:31707000-31708400	Active TSS	HSMMtube	muscle
34	chr6:31707000-31709000	Enhancers	Fetal Brain Male	brain
35	chr6:31707000-31709200	Active TSS	Brain Germinal Matrix	brain
36	chr6:31707200-31707600	Flanking Active TSS	Primary T cells from cord blood	blood
37	chr6:31707200-31707600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
38	chr6:31707200-31707600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr6:31707200-31707600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr6:31707200-31707600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr6:31707200-31707600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr6:31707200-31707600	Flanking Active TSS	Stomach Smooth Muscle	stomach
43	chr6:31707200-31707600	Flanking Active TSS	Osteobl	bone
44	chr6:31707200-31707800	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr6:31707200-31707800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:31707200-31707800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:31707200-31707800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr6:31707200-31707800	Weak transcription	Small Intestine	intestine
49	chr6:31707200-31708000	Active TSS	H1 Cell Line	embryonic stem cell
50	chr6:31707200-31708000	Active TSS	Right Ventricle	heart

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