Variant report

Variant	rs2183947
Chromosome Location	chr6:26159356-26159357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:0)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MEF2A	chr6:26156360-26159557	K562	blood:	n/a	chr6:26158140-26158151 chr6:26158136-26158157 chr6:26158261-26158276 chr6:26158261-26158278 chr6:26158136-26158157 chr6:26158136-26158157 chr6:26158141-26158150 chr6:26158137-26158153 chr6:26156409-26156423 chr6:26158138-26158153 chr6:26158263-26158278 chr6:26158933-26158941
2	GATA3	chr6:26156280-26159538	A549	lung:	n/a	chr6:26158931-26158941
3	POLR2A	chr6:26156287-26160737	GM12878	blood:	n/a	n/a
4	MBD4	chr6:26156346-26159433	HepG2	liver:	n/a	n/a
5	POLR2A	chr6:26156355-26159394	GM18505	blood:	n/a	n/a
6	POLR2A	chr6:26156191-26159464	U87	brain:	n/a	n/a
7	PML	chr6:26158706-26159432	MCF-7	breast:	n/a	n/a
8	CHD2	chr6:26158946-26159529	Hela-S3	cervix:	n/a	n/a
9	ZNF143	chr6:26158798-26159442	K562	blood:	n/a	n/a
10	POLR2A	chr6:26156392-26162162	K562	blood:	n/a	n/a
11	TAF1	chr6:26159252-26159441	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr6:26156252-26159454	GM12891	blood:	n/a	n/a
13	POLR2A	chr6:26156218-26160153	ECC-1	luminal epithelium:	n/a	n/a
14	ZBTB33	chr6:26156266-26159508	SK-N-SH	brain:	n/a	n/a
15	SIN3AK20	chr6:26156280-26159915	SK-N-SH	brain:	n/a	n/a
16	RUNX3	chr6:26156276-26159357	GM12878	blood:	n/a	n/a
17	REST	chr6:26159046-26159406	K562	blood:	n/a	n/a
18	MAX	chr6:26156243-26159413	HCT-116	colon:	n/a	n/a
19	SIN3A	chr6:26156366-26160075	H1-hESC	embryonic stem cell:	n/a	chr6:26156537-26156550
20	POLR2A	chr6:26156305-26159909	K562	blood:	n/a	n/a
21	TCF12	chr6:26156152-26159509	SK-N-SH	brain:	n/a	n/a
22	TAF1	chr6:26158952-26159359	GM12878	blood:	n/a	n/a
23	PML	chr6:26155695-26161197	K562	blood:	n/a	n/a
24	POLR2A	chr6:26156229-26159486	ProgFib	skin:	n/a	n/a
25	POLR2A	chr6:26156199-26160105	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr6:26156326-26159915	HCT-116	colon:	n/a	n/a
27	SIN3AK20	chr6:26156248-26159917	HCT-116	colon:	n/a	n/a
28	MBD4	chr6:26156297-26159743	HepG2	liver:	n/a	n/a
29	POLR2A	chr6:26156370-26159431	GM19099	blood:	n/a	n/a
30	TAF1	chr6:26158813-26159436	SK-N-SH	brain:	n/a	n/a
31	SIN3AK20	chr6:26155606-26159453	MCF-7	breast:	n/a	n/a
32	POLR2A	chr6:26156106-26160036	HepG2	liver:	n/a	n/a
33	POLR2A	chr6:26156267-26159712	GM12892	blood:	n/a	n/a
34	POLR2A	chr6:26156339-26159445	SK-N-SH	brain:	n/a	n/a
35	POLR2A	chr6:26156285-26159926	SK-N-MC	brain:	n/a	n/a
36	POLR2A	chr6:26156238-26163035	K562	blood:	n/a	n/a
37	POLR2A	chr6:26156156-26160777	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr6:26156326-26162143	K562	blood:	n/a	n/a
39	WRNIP1	chr6:26159206-26159840	GM12878	blood:	n/a	n/a
40	MAZ	chr6:26158874-26159907	GM12878	blood:	n/a	n/a
41	ELK1	chr6:26158944-26159475	K562	blood:	n/a	n/a
42	POLR2A	chr6:26156263-26159441	HepG2	liver:	n/a	n/a
43	ZBTB33	chr6:26156308-26159403	A549	lung:	n/a	n/a
44	NRF1	chr6:26158936-26159400	H1-hESC	embryonic stem cell:	n/a	n/a
45	SP1	chr6:26156142-26159873	HCT-116	colon:	n/a	chr6:26159200-26159212 chr6:26159202-26159211 chr6:26157376-26157386 chr6:26157936-26157949 chr6:26157375-26157387 chr6:26157408-26157417 chr6:26157375-26157387 chr6:26156516-26156527 chr6:26158206-26158227 chr6:26159201-26159210 chr6:26157376-26157386 chr6:26159356-26159365
46	MAFK	chr6:26156368-26159375	Hela-S3	cervix:	n/a	chr6:26158783-26158798
47	JUND	chr6:26156313-26159434	HCT-116	colon:	n/a	chr6:26157943-26157952 chr6:26157942-26157951
48	NFIC	chr6:26156236-26159425	GM12878	blood:	n/a	n/a
49	ETS1	chr6:26157027-26159456	A549	lung:	n/a	n/a
50	POLR2A	chr6:26156185-26159488	U87	brain:	n/a	n/a

No data

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:1438486..1441264-chr6:26157588..26160281,2	K562	blood:
2	chr20:45981040..45982698-chr6:26158330..26160765,2	MCF-7	breast:
3	chr6:26158231..26160273-chr6:26456660..26458707,2	K562	blood:
4	chr17:56736342..56737984-chr6:26158889..26160717,2	MCF-7	breast:
5	chr6:26158796..26160362-chr6:28889736..28891430,2	MCF-7	breast:
6	chr6:26154851..26161490-chr6:27803982..27809302,10	MCF-7	breast:
7	chr6:26157128..26159753-chr6:26519202..26521718,3	K562	blood:
8	chr6:26159110..26159916-chr9:91927629..91928196,2	Hela-S3	cervix:
9	chr6:26155821..26161666-chr6:26595746..26599191,6	K562	blood:
10	chr4:129731326..129732115-chr6:26158771..26159658,2	Hela-S3	cervix:
11	chr17:59475282..59476864-chr6:26159025..26161358,2	MCF-7	breast:
12	chr1:113161705..113162355-chr6:26158558..26159489,2	Hela-S3	cervix:
13	chr6:7541573..7543305-chr6:26157976..26160637,2	MCF-7	breast:
14	chr6:26157754..26159719-chrX:40035587..40037677,2	K562	blood:
15	chr11:62553654..62556441-chr6:26158091..26159898,2	MCF-7	breast:
16	chr17:39844898..39846717-chr6:26157632..26159911,2	MCF-7	breast:
17	chr6:26158606..26161579-chr6:26427700..26429391,2	K562	blood:
18	chr17:57917729..57920994-chr6:26157290..26159599,3	MCF-7	breast:
19	chr6:26157950..26159489-chr6:26216516..26217479,4	Hela-S3	cervix:
20	chr4:74961279..74961967-chr6:26158517..26159473,2	Hela-S3	cervix:
21	chr6:26156539..26159752-chr6:27789792..27793850,5	MCF-7	breast:
22	chr3:196294148..196296034-chr6:26157528..26159567,2	MCF-7	breast:
23	chr6:26041051..26050922-chr6:26154916..26161227,19	MCF-7	breast:
24	chr6:26156157..26159561-chr6:27098059..27103137,9	MCF-7	breast:
25	chr12:51157529..51159205-chr6:26158256..26159760,2	MCF-7	breast:
26	chr10:16478865..16480731-chr6:26157879..26159983,2	MCF-7	breast:
27	chr6:26154955..26159424-chr6:27857638..27862895,13	MCF-7	breast:
28	chr6:26158395..26159375-chr7:100026037..100026741,2	NB4	blood:
29	chr6:26154897..26160424-chr6:27112363..27117818,13	MCF-7	breast:
30	chr6:26155265..26160650-chr6:27098824..27104648,17	MCF-7	breast:
31	chr20:26188947..26190833-chr6:26156720..26159562,2	MCF-7	breast:
32	chr6:26158181..26160251-chr7:139476447..139479207,2	K562	blood:
33	chr6:26155301..26160613-chr6:27781458..27785146,6	MCF-7	breast:
34	chr17:59432229..59434125-chr6:26159107..26161207,2	MCF-7	breast:
35	chr11:116643751..116644528-chr6:26158445..26159440,2	Hela-S3	cervix:
36	chr6:26157592..26159745-chr6:27777609..27780154,2	MCF-7	breast:
37	chr21:44344300..44346121-chr6:26158253..26159810,2	MCF-7	breast:
38	chr1:145381395..145383043-chr6:26157864..26159582,2	MCF-7	breast:
39	chr5:90676180..90677768-chr6:26156663..26159404,2	MCF-7	breast:
40	chr3:150480563..150481545-chr6:26158552..26159384,2	Hela-S3	cervix:
41	chr1:44114681..44117088-chr6:26156929..26159883,2	MCF-7	breast:
42	chr11:62620888..62622657-chr6:26157901..26159977,2	K562	blood:
43	chr6:26051079..26061905-chr6:26152751..26161537,32	MCF-7	breast:
44	chr6:26157345..26159809-chr6:26595346..26597752,3	K562	blood:
45	chr1:149858556..149861463-chr6:26159050..26161817,2	MCF-7	breast:
46	chr6:26158037..26160369-chr6:27440864..27442625,2	K562	blood:
47	chr2:38976206..38978531-chr6:26156385..26159468,3	MCF-7	breast:
48	chr6:26155271..26161648-chr6:27095163..27104437,21	K562	blood:
49	chr6:26019525..26036768-chr6:26154463..26163826,38	MCF-7	breast:
50	chr6:26155235..26159457-chr6:27110736..27118010,14	K562	blood:

No data

Variant related genes	Relation type
LARP1P1	TF binding region
ENSG00000184825	Chromatin interaction
ENSG00000096654	Chromatin interaction
ENSG00000255717	Chromatin interaction
ENSG00000268798	Chromatin interaction
ENSG00000196532	Chromatin interaction
ENSG00000227195	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000007341	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000185798	Chromatin interaction
ENSG00000181788	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000115875	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000165983	Chromatin interaction
ENSG00000115268	Chromatin interaction
ENSG00000113369	Chromatin interaction
ENSG00000174013	Chromatin interaction
ENSG00000064393	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000096696	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000059377	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000123268	Chromatin interaction
ENSG00000066135	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000233056	Chromatin interaction
ENSG00000226645	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000196226	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000231119	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000183337	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000112763	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000146109	Chromatin interaction
ENSG00000116489	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000197238	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000173812	Chromatin interaction
ENSG00000234816	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000204713	Chromatin interaction
ENSG00000184348	Chromatin interaction
ENSG00000197903	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1009181	0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1059490	0.84[ASN][1000 genomes]
rs17598927	0.82[YRI][hapmap]
rs2066295	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4486004	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];0.92[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72834694	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72834696	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs806973	0.88[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs9358909	0.83[AMR][1000 genomes]
rs9366639	0.82[CEU][hapmap];1.00[CHD][hapmap];0.93[MEX][hapmap];0.81[AMR][1000 genomes]
rs9379827	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9379828	0.84[ASN][1000 genomes]
rs9379829	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.92[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9379830	1.00[CEU][hapmap];0.81[CHB][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9379831	0.80[CEU][hapmap];0.86[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv1028456	chr6:25984457-26174993	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
8	nsv538165	chr6:25984457-26174993	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	873 gene(s)	inside rSNPs	diseases
9	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
10	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
11	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
12	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
13	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
14	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
15	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
16	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
17	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
18	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
19	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
20	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs2183947	HIST1H1C	cis	parietal	SCAN
rs2183947	SCGN	cis	parietal	SCAN
rs2183947	HIST1H3H	cis	parietal	SCAN
rs2183947	HIST1H4H	cis	parietal	SCAN
rs2183947	ZSCAN23	cis	cerebellum	SCAN
rs2183947	HIST1H2BJ	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26155400-26160800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:26155600-26159600	Active TSS	Fetal Lung	lung
3	chr6:26155600-26159600	Active TSS	Psoas Muscle	Psoas
4	chr6:26155600-26159800	Active TSS	Fetal Kidney	kidney
5	chr6:26155600-26159800	Active TSS	HSMMtube	muscle
6	chr6:26155600-26160000	Active TSS	Brain Cingulate Gyrus	brain
7	chr6:26155600-26160600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:26155600-26160800	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr6:26155800-26159600	Active TSS	Colon Smooth Muscle	Colon
10	chr6:26155800-26159600	Active TSS	Right Ventricle	heart
11	chr6:26155800-26159600	Active TSS	Sigmoid Colon	Sigmoid Colon
12	chr6:26155800-26159800	Active TSS	Breast Myoepithelial Primary Cells	Breast
13	chr6:26155800-26159800	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr6:26155800-26160000	Active TSS	H9 Cell Line	embryonic stem cell
15	chr6:26155800-26160000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:26155800-26160000	Active TSS	Placenta Amnion	Placenta Amnion
17	chr6:26155800-26160200	Active TSS	HUES6 Cell Line	embryonic stem cell
18	chr6:26155800-26160200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:26155800-26160200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr6:26155800-26160200	Active TSS	Fetal Intestine Large	intestine
21	chr6:26155800-26160200	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr6:26155800-26160200	Active TSS	A549	lung
23	chr6:26155800-26160200	Active TSS	HSMM	muscle
24	chr6:26155800-26160400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr6:26155800-26160400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:26155800-26160400	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr6:26155800-26160400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:26155800-26160400	Active TSS	Pancreas	Pancrea
29	chr6:26155800-26160600	Active TSS	H1 Cell Line	embryonic stem cell
30	chr6:26155800-26160600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:26155800-26160600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:26155800-26160600	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr6:26155800-26160800	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr6:26155800-26160800	Active TSS	Colonic Mucosa	Colon
35	chr6:26155800-26161200	Active TSS	Thymus	Thymus
36	chr6:26156000-26159600	Active TSS	Left Ventricle	heart
37	chr6:26156000-26159600	Active TSS	Rectal Smooth Muscle	rectum
38	chr6:26156000-26159800	Active TSS	Primary B cells from peripheral blood	blood
39	chr6:26156000-26159800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:26156000-26159800	Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr6:26156000-26159800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:26156000-26159800	Active TSS	Brain Anterior Caudate	brain
43	chr6:26156000-26159800	Active TSS	HMEC	breast
44	chr6:26156000-26160000	Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr6:26156000-26160000	Active TSS	Stomach Mucosa	stomach
46	chr6:26156000-26160200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:26156000-26160200	Active TSS	Brain Substantia Nigra	brain
48	chr6:26156000-26160200	Active TSS	Esophagus	oesophagus
49	chr6:26156000-26160200	Active TSS	NHLF	lung
50	chr6:26156000-26160400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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