Variant report

Variant	rs3752416
Chromosome Location	chr6:26045929-26045930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:0)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr6:26045916-26045973	MCF-7	breast:	n/a	n/a
2	REST	chr6:26045445-26045994	SK-N-SH	brain:	n/a	n/a
3	CTCF	chr6:26045880-26046030	HMF	breast:	n/a	n/a
4	BATF	chr6:26045501-26045967	GM12878	blood:	n/a	n/a
5	POLR2A	chr6:26043180-26046720	GM12892	blood:	n/a	n/a
6	CTCF	chr6:26045820-26045970	HRE	kidney:	n/a	n/a
7	NFIC	chr6:26043271-26046700	GM12878	blood:	n/a	n/a
8	ELK4	chr6:26045679-26045995	Hela-S3	cervix:	n/a	chr6:26045825-26045836
9	ELF1	chr6:26045514-26046144	HepG2	liver:	n/a	n/a
10	CTCF	chr6:26045761-26046029	MCF-7	breast:	n/a	n/a
11	YY1	chr6:26045447-26046159	GM12878	blood:	n/a	n/a
12	KAT2A	chr6:26045530-26046601	GM12878	blood:	n/a	n/a
13	ELF1	chr6:26045393-26046154	GM12878	blood:	n/a	n/a
14	MXI1	chr6:26043247-26046992	IMR90	lung:	n/a	n/a
15	FOXM1	chr6:26045075-26046600	GM12878	blood:	n/a	n/a
16	RAD21	chr6:26045639-26046135	HepG2	liver:	n/a	n/a
17	CTCF	chr6:26045780-26045930	AG09309	skin:	n/a	n/a
18	CTCF	chr6:26045800-26045950	GM12875	blood:	n/a	n/a
19	CTCF	chr6:26045860-26046010	SK-N-SH_RA	brain:	n/a	n/a
20	POLR2A	chr6:26043122-26046798	SK-N-SH	brain:	n/a	n/a
21	POLR2A	chr6:26043135-26046646	HUVEC	blood vessel:	n/a	n/a
22	YY1	chr6:26045559-26046190	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:26045296-26045988	HepG2	liver:	n/a	chr6:26045517-26045525
24	MEF2C	chr6:26045432-26046361	GM12878	blood:	n/a	n/a
25	MEF2A	chr6:26045286-26046024	GM12878	blood:	n/a	n/a
26	CHD2	chr6:26045416-26046150	HepG2	liver:	n/a	n/a
27	ETS1	chr6:26045356-26046349	GM12878	blood:	n/a	n/a
28	ELF1	chr6:26045564-26046042	GM12878	blood:	n/a	n/a
29	CTCF	chr6:26045804-26046003	A549	lung:	n/a	n/a
30	SIN3AK20	chr6:26045328-26046368	HepG2	liver:	n/a	n/a
31	USF2	chr6:26045635-26046107	HepG2	liver:	n/a	n/a
32	CTCF	chr6:26045880-26046030	HPAF	blood vessel:	n/a	n/a
33	RELA	chr6:26045220-26046468	GM18505	blood:	n/a	n/a
34	POLR2A	chr6:26043226-26046775	U87	brain:	n/a	n/a
35	CTCF	chr6:26045860-26046010	GM12866	blood:	n/a	n/a
36	HEY1	chr6:26045660-26046106	K562	blood:	n/a	n/a
37	POLR2A	chr6:26043081-26046720	GM12892	blood:	n/a	n/a
38	JUND	chr6:26045529-26045997	HepG2	liver:	n/a	chr6:26045559-26045568
39	POLR2A	chr6:26043204-26046824	GM12878	blood:	n/a	n/a
40	CTCF	chr6:26045860-26046010	AG09319	gingival:	n/a	n/a
41	CTCF	chr6:26045761-26046125	GM12878	blood:	n/a	n/a
42	POLR2A	chr6:26043051-26046692	U87	brain:	n/a	n/a
43	CEBPB	chr6:26045355-26046608	Hela-S3	cervix:	n/a	chr6:26045517-26045525
44	CTCF	chr6:26045840-26045990	HFF	foreskin:	n/a	n/a
45	POLR2A	chr6:26045360-26046640	GM12878	blood:	n/a	n/a
46	MAFF	chr6:26045416-26046019	HepG2	liver:	n/a	n/a
47	ETS1	chr6:26045429-26046216	GM12878	blood:	n/a	n/a
48	NFATC1	chr6:26044958-26046598	GM12878	blood:	n/a	n/a
49	MYC	chr6:26045678-26045979	MCF-7	breast:	n/a	n/a
50	YY1	chr6:26045475-26045976	GM12892	blood:	n/a	n/a

No data

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26044671..26047980-chr6:26183838..26186075,3	MCF-7	breast:
2	chr6:26044692..26047309-chr6:27838299..27842021,15	MCF-7	breast:
3	chr11:62608525..62609492-chr6:26044962..26046193,3	Hela-S3	cervix:
4	chr6:26044090..26046416-chr6:26198004..26201095,3	MCF-7	breast:
5	chr6:26045430..26046056-chr6:27839789..27840289,2	MCF-7	breast:
6	chr22:21355852..21356503-chr6:26045280..26046103,2	Hela-S3	cervix:
7	chr6:26044265..26046503-chr6:27834017..27836277,2	MCF-7	breast:
8	chr16:778331..779043-chr6:26045506..26046071,2	Hela-S3	cervix:
9	chr6:26044049..26046588-chr6:26248373..26251129,2	MCF-7	breast:
10	chr17:56708294..56710638-chr6:26044705..26047582,3	MCF-7	breast:
11	chr2:176033004..176033600-chr6:26045198..26046133,2	NB4	blood:
12	chr17:56736144..56737118-chr6:26045265..26045991,2	Hela-S3	cervix:
13	chr6:26045666..26048095-chr6:26203965..26208002,5	MCF-7	breast:
14	chr5:108083905..108084789-chr6:26045639..26046332,2	NB4	blood:
15	chr6:26033327..26033948-chr6:26045432..26046107,2	NB4	blood:
16	chr6:26045293..26047313-chr6:35435617..35437589,2	MCF-7	breast:
17	chr6:26033393..26033930-chr6:26045556..26046130,2	Hela-S3	cervix:
18	chr1:41157343..41158090-chr6:26045452..26046059,2	NB4	blood:
19	chr6:26044526..26047786-chr6:27838310..27841317,7	MCF-7	breast:
20	chr6:26045566..26046278-chr6:27839320..27840308,2	MCF-7	breast:
21	chr6:26041051..26050922-chr6:26154916..26161227,19	MCF-7	breast:
22	chr15:63568954..63569918-chr6:26045477..26046174,2	NB4	blood:
23	chr6:26044121..26047112-chr6:27113025..27116157,4	MCF-7	breast:
24	chr6:26043872..26047495-chr6:26122651..26127553,11	MCF-7	breast:
25	chr6:26045094..26046041-chr9:74979546..74980409,3	Hela-S3	cervix:
26	chr6:26043570..26047536-chr6:26215421..26218540,6	MCF-7	breast:
27	chr6:26045221..26046099-chr6:27839800..27840316,5	Hela-S3	cervix:

No data

Variant related genes	Relation type
HIST1H2BB	TF binding region
ENSG00000066136	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000184436	Chromatin interaction
ENSG00000198518	Chromatin interaction
ENSG00000198755	Chromatin interaction
ENSG00000103253	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000138613	Chromatin interaction
ENSG00000115966	Chromatin interaction
ENSG00000196866	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000272145	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000107372	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000197846	Chromatin interaction
ENSG00000184357	Chromatin interaction
ENSG00000230513	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000197697	Chromatin interaction
ENSG00000256316	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000151422	Chromatin interaction
ENSG00000182572	Chromatin interaction
ENSG00000198558	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10425	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1090947	0.82[ASN][1000 genomes]
rs12346	0.81[EUR][1000 genomes]
rs1540275	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1540276	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1935235	0.89[EUR][1000 genomes]
rs199750	0.83[EUR][1000 genomes]
rs199751	0.83[EUR][1000 genomes]
rs199752	0.82[EUR][1000 genomes]
rs2032447	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2213284	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2230655	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34413295	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4291093	0.88[ASN][1000 genomes]
rs4401650	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6901039	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6922788	0.81[EUR][1000 genomes]
rs6942072	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7756117	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7760848	0.86[EUR][1000 genomes]
rs807212	0.89[EUR][1000 genomes]
rs9295683	0.92[AFR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9356995	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9358901	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9379822	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9467664	0.81[AMR][1000 genomes];0.87[EUR][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	nsv432857	chr6:25957109-26072445	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	451 gene(s)	inside rSNPs	diseases
8	nsv1015627	chr6:25973495-26100483	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
9	nsv538164	chr6:25973495-26100483	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	447 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	nsv1026692	chr6:26027408-26067081	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	363 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26034400-26048200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:26043000-26046600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr6:26043200-26046000	Active TSS	Colon Smooth Muscle	Colon
4	chr6:26043200-26046200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:26043200-26046200	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr6:26043200-26046200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr6:26043200-26046200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:26043200-26046200	Active TSS	Brain Anterior Caudate	brain
9	chr6:26043200-26046400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:26043200-26046400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:26043200-26046600	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr6:26043200-26046600	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr6:26043200-26046600	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr6:26043200-26046800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:26043400-26046000	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr6:26043400-26046000	Active TSS	HSMMtube	muscle
17	chr6:26043400-26046200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr6:26043400-26046400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:26043400-26046600	Active TSS	H9 Cell Line	embryonic stem cell
20	chr6:26043400-26046600	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr6:26043400-26046600	Active TSS	A549	lung
22	chr6:26043400-26046600	Flanking Active TSS	NHEK	skin
23	chr6:26043600-26046200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:26043800-26046000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:26043800-26046000	Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr6:26043800-26046000	Active TSS	Hela-S3	cervix
27	chr6:26043800-26046200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr6:26043800-26046400	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr6:26043800-26046400	Active TSS	NHDF-Ad	bronchial
30	chr6:26043800-26046600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:26044000-26046000	Active TSS	Fetal Heart	heart
32	chr6:26044200-26046000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
33	chr6:26044200-26046000	Active TSS	Small Intestine	intestine
34	chr6:26044200-26046200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr6:26044200-26046200	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr6:26044200-26046200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:26044200-26046600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:26044200-26046600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:26044200-26046600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr6:26044200-26046600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr6:26044200-26046600	Flanking Active TSS	HMEC	breast
42	chr6:26044200-26046800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr6:26044400-26046000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:26044600-26054800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:26044600-26055000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:26045000-26046600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr6:26045200-26046200	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr6:26045200-26046400	Active TSS	Brain Germinal Matrix	brain
49	chr6:26045400-26046200	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr6:26045400-26046200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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