Variant report

Variant	rs117756257
Chromosome Location	chr1:155196558-155196559
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:455)
CpG islands
(count:0)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCFL	chr1:155196458-155196665	K562	blood:	n/a	n/a
2	CTCF	chr1:155196460-155196610	MCF-7	breast:	n/a	n/a
3	CTCF	chr1:155196540-155196690	GM06990	blood:	n/a	n/a
4	MAFK	chr1:155196253-155196869	K562	blood:	n/a	n/a
5	CTCF	chr1:155196500-155196650	HPAF	blood vessel:	n/a	n/a
6	HA-E2F1	chr1:155196419-155197878	Hela-S3	cervix:	n/a	chr1:155197510-155197519 chr1:155197528-155197535 chr1:155197333-155197342 chr1:155197528-155197535 chr1:155197234-155197241 chr1:155197528-155197535 chr1:155197527-155197539
7	POLR2A	chr1:155196073-155198028	U87	brain:	n/a	n/a
8	CTCF	chr1:155196500-155196650	Caco-2	colon:	n/a	n/a
9	TEAD4	chr1:155196085-155198008	K562	blood:	n/a	n/a
10	TBP	chr1:155196355-155198033	H1-hESC	embryonic stem cell:	n/a	n/a
11	ELK4	chr1:155196227-155198211	Hela-S3	cervix:	n/a	n/a
12	MAFK	chr1:155196222-155198060	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr1:155196242-155197046	ECC-1	luminal epithelium:	n/a	n/a
14	CTCF	chr1:155196520-155196670	HL-60	blood:	n/a	n/a
15	MAX	chr1:155196281-155197954	ECC-1	luminal epithelium:	n/a	chr1:155197553-155197563 chr1:155197239-155197248
16	CTCF	chr1:155196392-155196780	IMR90	lung:	n/a	n/a
17	CTCF	chr1:155196358-155196767	K562	blood:	n/a	n/a
18	POLR2A	chr1:155196150-155198017	Hela-S3	cervix:	n/a	n/a
19	ZNF143	chr1:155196206-155197859	Hela-S3	cervix:	n/a	n/a
20	RAD21	chr1:155196389-155196806	IMR90	lung:	n/a	n/a
21	CTCF	chr1:155196455-155196748	Spleen_OC	spleen:	n/a	n/a
22	MAZ	chr1:155196311-155197888	GM12878	blood:	n/a	chr1:155197553-155197563 chr1:155197239-155197248
23	CTCF	chr1:155196540-155196690	GM12867	blood:	n/a	n/a
24	CTCF	chr1:155196152-155197604	HCT-116	colon:	n/a	n/a
25	EP300	chr1:155196244-155198034	K562	blood:	n/a	chr1:155197209-155197218
26	BACH1	chr1:155196500-155196997	K562	blood:	n/a	n/a
27	MXI1	chr1:155196465-155197680	HepG2	liver:	n/a	n/a
28	POLR2A	chr1:155196317-155196561	MCF10A-Er-Src	breast:	n/a	n/a
29	GTF2B	chr1:155196402-155196759	K562	blood:	n/a	n/a
30	SP4	chr1:155196349-155198001	H1-hESC	embryonic stem cell:	n/a	chr1:155197335-155197351 chr1:155197548-155197559
31	TCF7L2	chr1:155196504-155197417	PANC-1	pancreas:	n/a	chr1:155196822-155196836 chr1:155196826-155196835 chr1:155197143-155197150
32	POLR2A	chr1:155196237-155197970	K562	blood:	n/a	n/a
33	RCOR1	chr1:155196210-155197929	K562	blood:	n/a	n/a
34	MAX	chr1:155196225-155197953	GM12878	blood:	n/a	chr1:155197553-155197563 chr1:155197239-155197248
35	POLR2A	chr1:155196158-155198160	K562	blood:	n/a	n/a
36	CTCF	chr1:155196520-155196670	HPAF	blood vessel:	n/a	n/a
37	POLR2A	chr1:155196266-155198116	GM12891	blood:	n/a	n/a
38	CTCF	chr1:155196520-155196670	GM12864	blood:	n/a	n/a
39	CTCF	chr1:155196500-155196650	HCFaa	heart:	n/a	n/a
40	POLR2A	chr1:155196268-155198077	PBDE	blood:	n/a	n/a
41	CTCF	chr1:155196460-155196610	HAc	cerebellar:	n/a	n/a
42	MYC	chr1:155196312-155197962	K562	blood:	n/a	chr1:155197553-155197563 chr1:155197239-155197248
43	CTCF	chr1:155196500-155196650	NHDF-neo	bronchial:	n/a	n/a
44	RCOR1	chr1:155196255-155198036	GM12878	blood:	n/a	n/a
45	YY1	chr1:155196284-155197985	GM12878	blood:	n/a	n/a
46	CTCF	chr1:155196440-155196590	AG04450	lung:	n/a	n/a
47	REST	chr1:155196392-155198115	HL-60	blood:	n/a	n/a
48	POLR2A	chr1:155196175-155197851	HUVEC	blood vessel:	n/a	n/a
49	MAX	chr1:155196181-155198085	K562	blood:	n/a	chr1:155197553-155197563 chr1:155197239-155197248
50	CTCF	chr1:155196495-155196709	GM10266	blood:	n/a	n/a

No data

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155143901..155153030-chr1:155191166..155199183,23	MCF-7	breast:
2	chr1:155187581..155189617-chr1:155195998..155199387,4	MCF-7	breast:
3	chr1:155098008..155101008-chr1:155194682..155198746,4	MCF-7	breast:
4	chr1:155176293..155177732-chr1:155196164..155197059,7	MCF-7	breast:
5	chr1:155187302..155192095-chr1:155195846..155198767,7	MCF-7	breast:
6	chr1:155165613..155168147-chr1:155195516..155197930,3	K562	blood:
7	chr1:155195759..155198427-chr1:155276824..155279493,2	K562	blood:
8	chr1:155022097..155024403-chr1:155195809..155198176,3	MCF-7	breast:
9	chr1:155171519..155180465-chr1:155194608..155199196,19	MCF-7	breast:
10	chr1:155196466..155197461-chr20:32254440..32254956,2	Hela-S3	cervix:
11	chr1:155194687..155197665-chr1:155223228..155225374,3	MCF-7	breast:
12	chr1:155169616..155173195-chr1:155194780..155198735,4	MCF-7	breast:
13	chr1:155186661..155189522-chr1:155194169..155197986,6	K562	blood:
14	chr1:155195600..155203152-chr1:155209955..155216515,9	MCF-7	breast:
15	chr1:155174605..155182734-chr1:155187211..155200915,43	MCF-7	breast:
16	chr1:155178151..155179039-chr1:155196306..155197423,3	Hela-S3	cervix:
17	chr1:155157869..155162042-chr1:155196023..155198721,3	MCF-7	breast:
18	chr1:155176536..155177291-chr1:155196359..155196911,2	MCF-7	breast:
19	chr1:155193544..155197336-chr1:155293049..155296583,5	MCF-7	breast:
20	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
21	chr1:155196524..155199471-chr1:155205933..155208728,2	MCF-7	breast:
22	chr1:155196517..155197108-chr12:46384125..46384821,2	Hela-S3	cervix:
23	chr1:155148823..155149771-chr1:155196116..155196635,2	K562	blood:
24	chr1:155177619..155178135-chr1:155196442..155197036,2	MCF-7	breast:
25	chr1:155146416..155150261-chr1:155194777..155198198,7	MCF-7	breast:
26	chr1:155195406..155199356-chr1:155210414..155216260,10	K562	blood:
27	chr1:155194530..155197215-chr1:155242223..155244850,3	K562	blood:
28	chr1:155195512..155198962-chr1:155200125..155202735,3	MCF-7	breast:
29	chr1:155191881..155194028-chr1:155195597..155197149,2	MCF-7	breast:
30	chr1:155148495..155149762-chr1:155196236..155196972,5	MCF-7	breast:
31	chr1:155143241..155145865-chr1:155194153..155197077,2	MCF-7	breast:
32	chr1:155149084..155150074-chr1:155196318..155196838,2	MCF-7	breast:
33	chr1:155106515..155109128-chr1:155196131..155198130,2	K562	blood:
34	chr1:155195599..155199380-chr1:155211353..155216703,7	MCF-7	breast:
35	chr1:155195691..155197531-chr1:155658226..155660788,2	K562	blood:
36	chr1:155195750..155198407-chr1:155276763..155279696,2	K562	blood:
37	chr1:155174590..155181850-chr1:155192419..155201858,28	K562	blood:
38	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
39	chr1:155192189..155193749-chr1:155195303..155196996,2	MCF-7	breast:
40	chr1:155176324..155177310-chr1:155196150..155197130,9	K562	blood:
41	chr1:155196402..155197362-chr16:89557375..89557938,2	Hela-S3	cervix:
42	chr1:155188805..155190957-chr1:155195706..155197646,3	K562	blood:
43	chr1:155162384..155165288-chr1:155195792..155197762,4	MCF-7	breast:
44	chr1:145381905..145382698-chr1:155196540..155197297,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
MTX1P1	TF binding region
ENSG00000160766	Chromatin interaction
ENSG00000236675	Chromatin interaction
ENSG00000169231	Chromatin interaction
ENSG00000160767	Chromatin interaction
ENSG00000231064	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000173171	Chromatin interaction
ENSG00000169242	Chromatin interaction
ENSG00000163374	Chromatin interaction
ENSG00000139218	Chromatin interaction
ENSG00000160752	Chromatin interaction
ENSG00000185499	Chromatin interaction
ENSG00000132676	Chromatin interaction
ENSG00000163463	Chromatin interaction
ENSG00000225855	Chromatin interaction
ENSG00000160753	Chromatin interaction
ENSG00000143537	Chromatin interaction
ENSG00000169241	Chromatin interaction
ENSG00000176444	Chromatin interaction
ENSG00000125967	Chromatin interaction
ENSG00000163462	Chromatin interaction
ENSG00000177628	Chromatin interaction
ENSG00000197912	Chromatin interaction
ENSG00000271748	Chromatin interaction
ENSG00000216109	Chromatin interaction
ENSG00000273088	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
2	esv1823746	chr1:154965207-155231904	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription 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	469 gene(s)	inside rSNPs	diseases
3	nsv831614	chr1:155094978-155275031	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	434 gene(s)	inside rSNPs	diseases
4	esv2757756	chr1:155094978-155314807	Bivalent Enhancer Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
5	esv2758971	chr1:155094978-155314807	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
6	nsv470741	chr1:155115260-155230131	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	381 gene(s)	inside rSNPs	diseases
7	nsv1010146	chr1:155119096-155201064	ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
8	nsv872457	chr1:155135335-155310443	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
9	nsv831625	chr1:155145634-155313409	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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 miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
10	nsv527682	chr1:155149718-155197462	Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	361 gene(s)	inside rSNPs	diseases
11	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
12	esv2764209	chr1:155175657-155201064	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv547963	chr1:155178746-155206167	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
14	nsv870053	chr1:155180349-155212316	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
15	esv13606	chr1:155180489-155221243	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
16	esv3373583	chr1:155183155-155203622	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
17	esv3409536	chr1:155183691-155204364	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
18	nsv8469	chr1:155183945-155204572	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
19	esv3394856	chr1:155184707-155205412	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
20	esv3435735	chr1:155184757-155203179	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
21	esv3692913	chr1:155185951-155204010	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
22	nsv547964	chr1:155185951-155204010	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
23	esv2421617	chr1:155185951-155206167	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
24	nsv870387	chr1:155187481-155205523	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
25	nsv514011	chr1:155189136-155197120	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	68 gene(s)	inside rSNPs	diseases
26	nsv1008748	chr1:155189148-155230610	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
27	nsv1011773	chr1:155189148-155234821	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
28	nsv441717	chr1:155189160-155201060	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	72 gene(s)	inside rSNPs	diseases
29	esv1803666	chr1:155189160-155201064	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
30	esv1814530	chr1:155189160-155201064	Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
31	esv2763713	chr1:155189160-155201064	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
32	esv3453089	chr1:155193228-155199226	Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	72 gene(s)	inside rSNPs	diseases
33	esv3453090	chr1:155193228-155199226	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	72 gene(s)	inside rSNPs	diseases
34	esv1793876	chr1:155194112-155212255	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	75 gene(s)	inside rSNPs	diseases
35	nsv516159	chr1:155194980-155197462	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	71 gene(s)	inside rSNPs	diseases
36	esv3397308	chr1:155195828-155200126	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	71 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155179600-155196600	Weak transcription	Gastric	stomach
2	chr1:155179600-155196600	Weak transcription	Small Intestine	intestine
3	chr1:155182200-155196600	Weak transcription	Lung	lung
4	chr1:155188600-155196600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr1:155192000-155196600	Enhancers	Primary B cells from peripheral blood	blood
6	chr1:155193600-155196600	Enhancers	Placenta	Placenta
7	chr1:155193800-155198200	Enhancers	Spleen	Spleen
8	chr1:155194600-155196600	Enhancers	Stomach Mucosa	stomach
9	chr1:155195400-155196600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:155195400-155196600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr1:155195400-155196600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:155195400-155197000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr1:155195400-155197000	Flanking Active TSS	Hela-S3	cervix
14	chr1:155195400-155197800	ZNF genes & repeats	Right Atrium	heart
15	chr1:155195600-155196600	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr1:155195600-155196600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr1:155195600-155196600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
18	chr1:155195600-155196800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:155195600-155197000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:155195600-155197800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:155195800-155196600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:155195800-155196600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:155195800-155196600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:155195800-155196600	Flanking Active TSS	Fetal Brain Female	brain
25	chr1:155195800-155196600	Flanking Active TSS	Dnd41	blood
26	chr1:155195800-155197200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr1:155195800-155197800	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr1:155196000-155196600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:155196000-155196600	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr1:155196000-155196600	Enhancers	Colon Smooth Muscle	Colon
31	chr1:155196000-155196600	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr1:155196000-155196600	Flanking Active TSS	HMEC	breast
33	chr1:155196000-155196600	Flanking Active TSS	HUVEC	blood vessel
34	chr1:155196000-155196600	Flanking Active TSS	NH-A	brain
35	chr1:155196000-155196600	Flanking Active TSS	NHDF-Ad	bronchial
36	chr1:155196000-155196600	Flanking Active TSS	NHLF	lung
37	chr1:155196000-155196800	Flanking Active TSS	Brain Germinal Matrix	brain
38	chr1:155196000-155197000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:155196000-155197000	Flanking Active TSS	NHEK	skin
40	chr1:155196000-155197000	Flanking Active TSS	Osteobl	bone
41	chr1:155196000-155197200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr1:155196000-155197200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr1:155196000-155197600	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr1:155196000-155197600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:155196000-155197600	Active TSS	GM12878-XiMat	blood
46	chr1:155196000-155197800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr1:155196200-155196600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:155196200-155196600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:155196200-155196600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr1:155196200-155196600	Flanking Active TSS	Brain Anterior Caudate	brain

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