Variant report

Variant	rs2298091
Chromosome Location	chr6:26158439-26158440
allele	A/C
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:151)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:41157264..41158156-chr6:26158172..26158794,2	Hela-S3	cervix:
2	chr6:26156738..26158730-chr6:26923909..26926382,2	K562	blood:
3	chr6:26157915..26159076-chr9:131314410..131315769,4	Hela-S3	cervix:
4	chr19:1438486..1441264-chr6:26157588..26160281,2	K562	blood:
5	chr11:72853178..72853964-chr6:26157634..26158477,2	Hela-S3	cervix:
6	chr4:1283187..1284079-chr6:26157656..26158585,2	NB4	blood:
7	chr20:45981040..45982698-chr6:26158330..26160765,2	MCF-7	breast:
8	chr12:69004663..69005179-chr6:26157790..26158604,2	Hela-S3	cervix:
9	chr19:34663756..34664272-chr6:26158379..26158914,2	Hela-S3	cervix:
10	chr14:23341421..23341991-chr6:26157911..26158480,2	Hela-S3	cervix:
11	chr19:58816331..58817188-chr6:26158029..26158817,2	Hela-S3	cervix:
12	chr20:5100074..5101027-chr6:26157868..26158439,2	NB4	blood:
13	chr6:26158231..26160273-chr6:26456660..26458707,2	K562	blood:
14	chr15:80351279..80352456-chr6:26158321..26159028,3	Hela-S3	cervix:
15	chr6:26158344..26159047-chr6:26199394..26200119,2	NB4	blood:
16	chr3:56716520..56717389-chr6:26157669..26158536,2	Hela-S3	cervix:
17	chr6:26021580..26022163-chr6:26157717..26158787,3	Hela-S3	cervix:
18	chr17:75136127..75136824-chr6:26158051..26158946,2	Hela-S3	cervix:
19	chr6:26154851..26161490-chr6:27803982..27809302,10	MCF-7	breast:
20	chr6:26157128..26159753-chr6:26519202..26521718,3	K562	blood:
21	chr6:26156544..26158635-chr9:115248573..115251037,2	MCF-7	breast:
22	chr6:26155821..26161666-chr6:26595746..26599191,6	K562	blood:
23	chr6:26158302..26159117-chr6:27775211..27776028,3	Hela-S3	cervix:
24	chr6:26158313..26158816-chr6:30711943..30712757,2	Hela-S3	cervix:
25	chr3:11761313..11762268-chr6:26157805..26158792,2	Hela-S3	cervix:
26	chr6:26158003..26158604-chr9:98078847..98079535,2	HCT-116	colon:
27	chr1:23857285..23857906-chr6:26157778..26158687,2	Hela-S3	cervix:
28	chr11:45168582..45169343-chr6:26157874..26158814,2	HCT-116	colon:
29	chr2:122288053..122289025-chr6:26157732..26158561,3	HCT-116	colon:
30	chr6:26157894..26158726-chr9:100000252..100000813,2	HCT-116	colon:
31	chr6:26156108..26158898-chr6:27832756..27836611,3	MCF-7	breast:
32	chr6:7541573..7543305-chr6:26157976..26160637,2	MCF-7	breast:
33	chr6:26123627..26125056-chr6:26157699..26158576,4	Hela-S3	cervix:
34	chr6:26157754..26159719-chrX:40035587..40037677,2	K562	blood:
35	chr11:62553654..62556441-chr6:26158091..26159898,2	MCF-7	breast:
36	chr1:155213935..155214771-chr6:26157834..26158708,2	Hela-S3	cervix:
37	chr6:26157535..26158525-chr6:30524230..30524818,2	Hela-S3	cervix:
38	chr20:48428781..48429688-chr6:26157889..26158656,2	Hela-S3	cervix:
39	chr17:39844898..39846717-chr6:26157632..26159911,2	MCF-7	breast:
40	chr6:26157950..26158889-chr6:112194335..112194894,2	Hela-S3	cervix:
41	chr3:186501413..186501997-chr6:26158281..26158811,2	Hela-S3	cervix:
42	chr6:26123837..26124686-chr6:26157659..26158968,4	HCT-116	colon:
43	chr1:151583782..151586135-chr6:26156499..26159013,2	MCF-7	breast:
44	chr17:6543742..6544252-chr6:26158048..26158799,2	Hela-S3	cervix:
45	chr4:84205500..84206046-chr6:26158335..26159311,2	Hela-S3	cervix:
46	chr15:65587900..65588835-chr6:26157581..26158604,4	Hela-S3	cervix:
47	chr17:57917729..57920994-chr6:26157290..26159599,3	MCF-7	breast:
48	chr17:42976358..42976871-chr6:26158243..26158951,2	Hela-S3	cervix:
49	chr6:26155577..26158576-chr9:91147501..91150274,2	MCF-7	breast:
50	chr17:79476638..79478396-chr6:26156378..26158994,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000214253	Chromatin interaction
ENSG00000137876	Chromatin interaction
ENSG00000197818	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000130699	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000151923	Chromatin interaction
ENSG00000212456	Chromatin interaction
ENSG00000197622	Chromatin interaction
ENSG00000198931	Chromatin interaction
ENSG00000263826	Chromatin interaction
ENSG00000261366	Chromatin interaction
ENSG00000165185	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000267858	Chromatin interaction
ENSG00000108106	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000086666	Chromatin interaction
ENSG00000173085	Chromatin interaction
ENSG00000175324	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000185798	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000073670	Chromatin interaction
ENSG00000167131	Chromatin interaction
ENSG00000156110	Chromatin interaction
ENSG00000143578	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000144560	Chromatin interaction
ENSG00000145632	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000137331	Chromatin interaction
ENSG00000026950	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000066135	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000196532	Chromatin interaction
ENSG00000176142	Chromatin interaction
ENSG00000156976	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000131653	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000082996	Chromatin interaction
ENSG00000143376	Chromatin interaction
ENSG00000241549	Chromatin interaction
ENSG00000233056	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000172469	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000234816	Chromatin interaction
ENSG00000156469	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000163660	Chromatin interaction
ENSG00000151422	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000156735	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000152348	Chromatin interaction
ENSG00000096654	Chromatin interaction
ENSG00000175283	Chromatin interaction
ENSG00000113240	Chromatin interaction
ENSG00000197459	Chromatin interaction
ENSG00000117543	Chromatin interaction
ENSG00000268798	Chromatin interaction
ENSG00000204576	Chromatin interaction
ENSG00000171222	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000132646	Chromatin interaction
ENSG00000250734	Chromatin interaction
ENSG00000019485	Chromatin interaction
ENSG00000188987	Chromatin interaction
ENSG00000243789	Chromatin interaction
ENSG00000264229	Chromatin interaction
ENSG00000206630	Chromatin interaction
ENSG00000203499	Chromatin interaction
ENSG00000184357	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000230185	Chromatin interaction
ENSG00000249915	Chromatin interaction
ENSG00000248925	Chromatin interaction
ENSG00000063176	Chromatin interaction
ENSG00000057608	Chromatin interaction
ENSG00000199568	Chromatin interaction
ENSG00000170545	Chromatin interaction
ENSG00000168710	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000113369	Chromatin interaction
ENSG00000143384	Chromatin interaction
ENSG00000259438	Chromatin interaction
ENSG00000198920	Chromatin interaction
ENSG00000063177	Chromatin interaction
ENSG00000074054	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000196262	Chromatin interaction
ENSG00000156471	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000197697	Chromatin interaction
ENSG00000255717	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000130045	Chromatin interaction
ENSG00000158169	Chromatin interaction
ENSG00000196226	Chromatin interaction
ENSG00000108883	Chromatin interaction
ENSG00000123136	Chromatin interaction
ENSG00000174013	Chromatin interaction
ENSG00000095319	Chromatin interaction
ENSG00000143458	Chromatin interaction
ENSG00000111144	Chromatin interaction
ENSG00000137478	Chromatin interaction
ENSG00000066136	Chromatin interaction
ENSG00000172301	Chromatin interaction
ENSG00000198374	Chromatin interaction
ENSG00000074356	Chromatin interaction
ENSG00000072401	Chromatin interaction
ENSG00000059377	Chromatin interaction
ENSG00000183337	Chromatin interaction
ENSG00000064393	Chromatin interaction
ENSG00000130309	Chromatin interaction
ENSG00000108107	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000172380	Chromatin interaction
ENSG00000238331	Chromatin interaction
ENSG00000260260	Chromatin interaction
ENSG00000123268	Chromatin interaction
ENSG00000096696	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000112763	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000266077	Chromatin interaction
ENSG00000166508	Chromatin interaction
ENSG00000104419	Chromatin interaction
ENSG00000069956	Chromatin interaction
ENSG00000115875	Chromatin interaction
ENSG00000266967	Chromatin interaction
ENSG00000173812	Chromatin interaction
ENSG00000227195	Chromatin interaction
ENSG00000233184	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000197238	Chromatin interaction
ENSG00000197816	Chromatin interaction
ENSG00000184348	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000163946	Chromatin interaction
ENSG00000018699	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000129657	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000129235	Chromatin interaction
ENSG00000197694	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000127314	Chromatin interaction
ENSG00000063046	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000204308	Chromatin interaction
ENSG00000178188	Chromatin interaction
ENSG00000010810	Chromatin interaction
ENSG00000231119	Chromatin interaction
ENSG00000176485	Chromatin interaction
ENSG00000115268	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000197324	Chromatin interaction
ENSG00000272145	Chromatin interaction
ENSG00000168970	Chromatin interaction
ENSG00000165983	Chromatin interaction
ENSG00000007968	Chromatin interaction
ENSG00000082641	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000228395	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000142396	Chromatin interaction
ENSG00000254876	Chromatin interaction
ENSG00000177628	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000243660	Chromatin interaction
ENSG00000224843	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000090316	Chromatin interaction
ENSG00000146109	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10484433	1.00[CHB][hapmap]
rs12111009	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs13196552	1.00[CHB][hapmap]
rs13220395	1.00[CHB][hapmap]
rs16891235	1.00[CHB][hapmap]
rs16891264	1.00[CHB][hapmap]
rs16891315	1.00[CHB][hapmap]
rs16891334	1.00[CHB][hapmap]
rs3734528	1.00[CHB][hapmap]
rs4476815	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs59324656	0.92[ASN][1000 genomes]
rs73393463	0.86[ASN][1000 genomes]
rs9467684	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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
21	nsv970083	chr6:26158290-26159152	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	239 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	chr6:26155400-26160800	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	chr6:26155800-26158800	Active TSS	K562	blood
10	chr6:26155800-26159600	Active TSS	Colon Smooth Muscle	Colon
11	chr6:26155800-26159600	Active TSS	Right Ventricle	heart
12	chr6:26155800-26159600	Active TSS	Sigmoid Colon	Sigmoid Colon
13	chr6:26155800-26159800	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr6:26155800-26159800	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr6:26155800-26160000	Active TSS	H9 Cell Line	embryonic stem cell
16	chr6:26155800-26160000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:26155800-26160000	Active TSS	Placenta Amnion	Placenta Amnion
18	chr6:26155800-26160200	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr6:26155800-26160200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:26155800-26160200	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr6:26155800-26160200	Active TSS	Fetal Intestine Large	intestine
22	chr6:26155800-26160200	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr6:26155800-26160200	Active TSS	A549	lung
24	chr6:26155800-26160200	Active TSS	HSMM	muscle
25	chr6:26155800-26160400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr6:26155800-26160400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:26155800-26160400	Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr6:26155800-26160400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr6:26155800-26160400	Active TSS	Pancreas	Pancrea
30	chr6:26155800-26160600	Active TSS	H1 Cell Line	embryonic stem cell
31	chr6:26155800-26160600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr6:26155800-26160600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr6:26155800-26160600	Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr6:26155800-26160800	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr6:26155800-26160800	Active TSS	Colonic Mucosa	Colon
36	chr6:26155800-26161200	Active TSS	Thymus	Thymus
37	chr6:26156000-26159000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:26156000-26159600	Active TSS	Left Ventricle	heart
39	chr6:26156000-26159600	Active TSS	Rectal Smooth Muscle	rectum
40	chr6:26156000-26159800	Active TSS	Primary B cells from peripheral blood	blood
41	chr6:26156000-26159800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr6:26156000-26159800	Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr6:26156000-26159800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:26156000-26159800	Active TSS	Brain Anterior Caudate	brain
45	chr6:26156000-26159800	Active TSS	HMEC	breast
46	chr6:26156000-26160000	Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr6:26156000-26160000	Active TSS	Stomach Mucosa	stomach
48	chr6:26156000-26160200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:26156000-26160200	Active TSS	Brain Substantia Nigra	brain
50	chr6:26156000-26160200	Active TSS	Esophagus	oesophagus

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