Variant report

Variant	rs201228591
Chromosome Location	chr6:31795833-31795834
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:31632509..31634091-chr6:31794981..31797016,2	MCF-7	breast:
2	chr6:31646374..31649912-chr6:31794618..31797680,6	MCF-7	breast:
3	chr6:31795413..31795934-chr9:117373017..117374000,2	Hela-S3	cervix:
4	chr6:31793170..31796834-chr6:31863715..31868848,6	K562	blood:
5	chr6:31795326..31798240-chr6:31869248..31870828,2	K562	blood:
6	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
7	chr10:72163649..72164159-chr6:31795462..31796020,2	NB4	blood:
8	chr6:31508088..31512302-chr6:31792582..31797881,5	K562	blood:
9	chr16:87425636..87426576-chr6:31795079..31795938,2	Hela-S3	cervix:
10	chr6:31794734..31796775-chr6:31868219..31871084,2	MCF-7	breast:
11	chr6:31508352..31511076-chr6:31794765..31796870,2	MCF-7	breast:
12	chr6:31795475..31798260-chr6:31864062..31867064,3	K562	blood:
13	chr5:43018130..43019042-chr6:31795467..31796002,2	Hela-S3	cervix:
14	chr6:31684129..31686897-chr6:31793349..31796953,3	MCF-7	breast:
15	chr6:31794061..31796965-chr6:32094661..32097719,3	K562	blood:
16	chr6:31793612..31800139-chr6:31830250..31833240,9	K562	blood:
17	chr14:31889308..31890174-chr6:31795417..31795943,2	Hela-S3	cervix:
18	chr16:89988437..89990274-chr6:31795215..31797917,2	MCF-7	breast:
19	chr6:31795636..31798245-chr6:31918876..31922534,3	MCF-7	breast:
20	chr6:31782320..31783797-chr6:31794894..31795956,19	Hela-S3	cervix:
21	chr6:31794807..31796884-chr6:31844966..31847954,2	MCF-7	breast:
22	chr6:31706679..31708956-chr6:31795250..31798080,2	MCF-7	breast:
23	chr6:31794009..31796794-chr6:31937769..31941181,3	K562	blood:
24	chr6:31619174..31622035-chr6:31794476..31797735,3	MCF-7	breast:
25	chr6:31686048..31689889-chr6:31795401..31797897,4	MCF-7	breast:
26	chr6:31793907..31797035-chr6:31916814..31918857,3	K562	blood:
27	chr6:31795638..31797726-chr6:32161977..32163708,2	K562	blood:
28	chr6:31743287..31747076-chr6:31793437..31796925,5	MCF-7	breast:
29	chr14:75745214..75745985-chr6:31795372..31795907,2	Hela-S3	cervix:
30	chr6:31508345..31511059-chr6:31794031..31797026,5	K562	blood:
31	chr6:31792517..31796452-chr6:31911867..31914768,3	MCF-7	breast:
32	chr10:38146501..38147130-chr6:31795044..31795963,2	Hela-S3	cervix:
33	chr6:31795039..31796009-chr6:33175540..33176385,2	Hela-S3	cervix:
34	chr6:31795540..31798054-chr6:31844082..31846588,3	K562	blood:
35	chr6:31793367..31797001-chr6:32936441..32941447,5	MCF-7	breast:
36	chr6:31795132..31795947-chr9:132245472..132246461,2	Hela-S3	cervix:
37	chr15:77223331..77224220-chr6:31795445..31796173,2	NB4	blood:
38	chr6:31698357..31701391-chr6:31793671..31797057,3	MCF-7	breast:
39	chr5:111496508..111497358-chr6:31795058..31795974,2	NB4	blood:
40	chr6:31782709..31783766-chr6:31794789..31796004,3	NB4	blood:
41	chr6:31782799..31783519-chr6:31795186..31795913,7	MCF-7	breast:
42	chr6:31794817..31797801-chr6:31829779..31831981,3	K562	blood:
43	chr6:31795174..31795954-chrX:23760489..23761485,2	Hela-S3	cervix:
44	chr20:49347653..49348478-chr6:31794981..31795951,2	MCF-7	breast:
45	chr16:2014337..2015106-chr6:31795311..31795999,2	Hela-S3	cervix:
46	chr15:30113789..30114693-chr6:31795054..31795835,2	Hela-S3	cervix:
47	chr6:31782095..31783822-chr6:31794892..31795963,5	MCF-7	breast:
48	chr6:31794076..31797070-chr6:31910942..31912443,2	K562	blood:
49	chr14:24898313..24899033-chr6:31795142..31796000,2	Hela-S3	cervix:
50	chr12:51632053..51632784-chr6:31795467..31796024,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000204344	Chromatin interaction
ENSG00000204420	Chromatin interaction
ENSG00000199036	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000255152	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000170345	Chromatin interaction
ENSG00000213676	Chromatin interaction
ENSG00000204257	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000255198	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000183283	Chromatin interaction
ENSG00000139899	Chromatin interaction
ENSG00000104067	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000100441	Chromatin interaction
ENSG00000117906	Chromatin interaction
ENSG00000140941	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000204227	Chromatin interaction
ENSG00000259006	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204428	Chromatin interaction
ENSG00000263756	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000129493	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000145901	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000251131	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204054	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000236514	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000213654	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000140988	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000250365	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000238363	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000103264	Chromatin interaction
ENSG00000204410	Chromatin interaction
ENSG00000198105	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000224032	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000148730	Chromatin interaction
ENSG00000123130	Chromatin interaction
ENSG00000204421	Chromatin interaction
ENSG00000157693	Chromatin interaction
ENSG00000258947	Chromatin interaction
ENSG00000234006	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:40 , 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	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
10	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
11	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
12	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
13	nsv884426	chr6:31728102-31800868	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv884427	chr6:31728102-31802465	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers 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 target site	152 gene(s)	inside rSNPs	diseases
15	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
16	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
17	nsv884430	chr6:31731881-31800631	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
18	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
19	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
20	nsv981359	chr6:31779004-31797103	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	111 gene(s)	inside rSNPs	diseases
21	nsv869989	chr6:31779203-31797657	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	114 gene(s)	inside rSNPs	diseases
22	nsv884450	chr6:31783527-31797769	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
23	nsv884451	chr6:31783527-31800631	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
24	esv3349739	chr6:31785205-31796114	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
25	esv2421830	chr6:31785228-31797422	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
26	nsv601947	chr6:31785228-31797422	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
27	nsv884454	chr6:31785228-31797422	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
28	nsv884455	chr6:31785228-31797422	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
29	nsv884456	chr6:31785228-31800631	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
30	nsv884457	chr6:31785228-31803130	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
31	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
32	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
33	nsv884460	chr6:31785453-31797422	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	90 gene(s)	inside rSNPs	diseases
34	nsv884461	chr6:31785453-31827045	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers 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 target site	117 gene(s)	inside rSNPs	diseases
35	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
36	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
37	nsv884462	chr6:31785792-31797422	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
38	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
39	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
40	esv3329350	chr6:31794973-31799171	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31794200-31796000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr6:31794200-31796000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:31794400-31796000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:31794400-31796000	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr6:31794400-31796000	Active TSS	Esophagus	oesophagus
6	chr6:31794600-31796000	Active TSS	H1 Cell Line	embryonic stem cell
7	chr6:31794600-31796000	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr6:31794600-31796000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:31794600-31796000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:31794600-31796000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:31794600-31796000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:31794600-31796000	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr6:31794600-31796000	Active TSS	Fetal Intestine Large	intestine
14	chr6:31794600-31796000	Active TSS	Left Ventricle	heart
15	chr6:31794600-31796000	Active TSS	Rectal Smooth Muscle	rectum
16	chr6:31794800-31796000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:31794800-31796000	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr6:31794800-31796000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr6:31794800-31796000	Active TSS	Primary hematopoietic stem cells short term culture	blood
20	chr6:31794800-31796000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:31794800-31796000	Active TSS	Muscle Satellite Cultured Cells	--
22	chr6:31794800-31796000	Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr6:31794800-31796000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr6:31794800-31796000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:31794800-31796000	Active TSS	Fetal Intestine Small	intestine
26	chr6:31794800-31796000	Active TSS	Fetal Muscle Leg	muscle
27	chr6:31794800-31796000	Active TSS	Fetal Stomach	stomach
28	chr6:31794800-31796000	Active TSS	Pancreas	Pancrea
29	chr6:31794800-31796000	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr6:31794800-31796000	Active TSS	Stomach Smooth Muscle	stomach
31	chr6:31794800-31796000	Active TSS	HMEC	breast
32	chr6:31794800-31796000	Active TSS	HSMM	muscle
33	chr6:31794800-31796000	Active TSS	Osteobl	bone
34	chr6:31795000-31796000	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr6:31795000-31796000	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr6:31795000-31796000	Active TSS	Primary monocytes fromperipheralblood	blood
37	chr6:31795000-31796000	Active TSS	Primary neutrophils fromperipheralblood	blood
38	chr6:31795000-31796000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:31795000-31796000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:31795000-31796000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:31795000-31796000	Active TSS	Brain Germinal Matrix	brain
42	chr6:31795000-31796000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr6:31795000-31796000	Active TSS	Fetal Kidney	kidney
44	chr6:31795000-31796000	Active TSS	Fetal Muscle Trunk	muscle
45	chr6:31795000-31796000	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr6:31795000-31796000	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr6:31795000-31796000	Active TSS	HepG2	liver
48	chr6:31795000-31796000	Active TSS	Monocytes-CD14+_RO01746	blood
49	chr6:31795000-31797400	Weak transcription	Fetal Heart	heart
50	chr6:31795200-31796000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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