Variant report

Variant	rs2283616
Chromosome Location	chr19:18682495-18682496
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr19:18682188-18682938	K562	blood:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
2	HDAC2	chr19:18682112-18682793	MCF-7	breast:	n/a	n/a
3	POLR2A	chr19:18682051-18683041	MCF-7	breast:	n/a	n/a
4	E2F4	chr19:18681638-18683070	MCF10A-Er-Src	breast:	n/a	chr19:18682942-18682954 chr19:18682479-18682488 chr19:18682621-18682630
5	GTF2F1	chr19:18682269-18682784	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr19:18682141-18683044	GM18505	blood:	n/a	n/a
7	YY1	chr19:18682366-18682745	HCT-116	colon:	n/a	chr19:18682542-18682564 chr19:18682560-18682571 chr19:18682555-18682563 chr19:18682548-18682565 chr19:18682547-18682566 chr19:18682554-18682564 chr19:18682553-18682561
8	UBTF	chr19:18682350-18683060	K562	blood:	n/a	n/a
9	EP300	chr19:18682235-18682738	GM12878	blood:	n/a	n/a
10	MYC	chr19:18682393-18682732	Hela-S3	cervix:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
11	TBL1XR1	chr19:18682281-18682879	GM12878	blood:	n/a	n/a
12	USF1	chr19:18682160-18682850	HCT-116	colon:	n/a	chr19:18682465-18682476 chr19:18682760-18682776
13	SP4	chr19:18682100-18682822	H1-hESC	embryonic stem cell:	n/a	n/a
14	YY1	chr19:18682386-18682670	K562	blood:	n/a	chr19:18682542-18682564 chr19:18682560-18682571 chr19:18682555-18682563 chr19:18682548-18682565 chr19:18682547-18682566 chr19:18682554-18682564 chr19:18682553-18682561
15	POLR2A	chr19:18682350-18682892	A549	lung:	n/a	n/a
16	MYC	chr19:18682308-18682924	K562	blood:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
17	POLR2A	chr19:18682097-18683045	H1-neurons	neurons:	n/a	n/a
18	MYC	chr19:18682146-18683014	A549	lung:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
19	TEAD4	chr19:18682252-18682904	K562	blood:	n/a	n/a
20	MYC	chr19:18682404-18682694	MCF-7	breast:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
21	USF1	chr19:18682347-18682775	SK-N-SH_RA	brain:	n/a	chr19:18682465-18682476
22	SIN3AK20	chr19:18682124-18683280	K562	blood:	n/a	n/a
23	NRF1	chr19:18682106-18682882	SK-N-SH	brain:	n/a	chr19:18682620-18682629 chr19:18682617-18682631 chr19:18682619-18682630 chr19:18682479-18682488 chr19:18682620-18682631
24	NFYA	chr19:18682348-18682693	Hela-S3	cervix:	n/a	n/a
25	FOXP2	chr19:18682335-18682961	PFSK-1	brain:	n/a	n/a
26	CEBPB	chr19:18682145-18682687	K562	blood:	n/a	n/a
27	POLR2A	chr19:18682135-18683047	GM19193	blood:	n/a	n/a
28	POLR2A	chr19:18681813-18682888	K562	blood:	n/a	n/a
29	CCNT2	chr19:18682353-18682985	K562	blood:	n/a	n/a
30	CREB1	chr19:18682128-18683143	GM12878	blood:	n/a	n/a
31	MYC	chr19:18682386-18682705	GM12878	blood:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
32	ETS1	chr19:18682324-18682736	A549	lung:	n/a	chr19:18682651-18682660 chr19:18682495-18682504 chr19:18682495-18682504 chr19:18682495-18682504 chr19:18682650-18682659 chr19:18682477-18682488 chr19:18682495-18682504 chr19:18682495-18682504 chr19:18682496-18682506 chr19:18682491-18682507 chr19:18682494-18682503 chr19:18682495-18682506 chr19:18682493-18682502 chr19:18682495-18682504 chr19:18682649-18682658
33	POLR2A	chr19:18681890-18683078	GM12878	blood:	n/a	n/a
34	SIX5	chr19:18682284-18682682	H1-hESC	embryonic stem cell:	n/a	n/a
35	MXI1	chr19:18682324-18683008	K562	blood:	n/a	chr19:18682519-18682528
36	STAT3	chr19:18682240-18682535	MCF10A-Er-Src	breast:	n/a	n/a
37	TAF1	chr19:18682141-18683127	ECC-1	luminal epithelium:	n/a	n/a
38	SIX5	chr19:18682271-18682700	K562	blood:	n/a	n/a
39	POLR2A	chr19:18682170-18682963	GM18951	blood:	n/a	n/a
40	MYC	chr19:18682309-18682794	Hela-S3	cervix:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
41	YY1	chr19:18682230-18683083	GM12878	blood:	n/a	chr19:18682542-18682564 chr19:18682560-18682571 chr19:18682555-18682563 chr19:18682548-18682565 chr19:18682547-18682566 chr19:18682554-18682564 chr19:18682553-18682561
42	POLR2A	chr19:18681493-18689919	HepG2	liver:	n/a	n/a
43	EGR1	chr19:18682424-18682638	GM12878	blood:	n/a	chr19:18682563-18682573 chr19:18682478-18682488 chr19:18682621-18682630
44	E2F4	chr19:18682243-18682754	GM12878	blood:	n/a	chr19:18682479-18682488 chr19:18682621-18682630
45	HCFC1	chr19:18682258-18683026	K562	blood:	n/a	n/a
46	MAZ	chr19:18682141-18683379	IMR90	lung:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
47	HDAC2	chr19:18682232-18682804	HepG2	liver:	n/a	n/a
48	MYC	chr19:18682295-18682769	K562	blood:	n/a	chr19:18682521-18682528 chr19:18682520-18682529 chr19:18682519-18682529
49	STAT5A	chr19:18682120-18682802	GM12878	blood:	n/a	n/a
50	RAD21	chr19:18682295-18682683	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18682484-18682534	GM19239	blood:	n/a
2	chr19:18682484-18682534	GM12878	blood:	n/a
3	chr19:18682480-18682530	HRE	kidney:	n/a
4	chr19:18682480-18682530	A549	lung:	n/a
5	chr19:18682484-18682534	PANC-1	pancreas:	n/a
6	chr19:18682463-18682513	HCM	heart:	n/a
7	chr19:18682463-18682513	HIPEpiC	eye:	n/a
8	chr19:18682480-18682530	ECC-1	luminal epithelium:	n/a
9	chr19:18682484-18682534	K562	blood:	n/a
10	chr19:18682484-18682534	ProgFib	skin:	n/a
11	chr19:18682484-18682534	H1-hESC	embryonic stem cell:	embryo
12	chr19:18682463-18682513	ovcar-3	ovarian:	n/a
13	chr19:18682484-18682534	MCF10A-Er-Src	breast:	n/a
14	chr19:18682463-18682513	ProgFib	skin:	n/a
15	chr19:18682463-18682513	CMK	blood:	n/a
16	chr19:18682463-18682513	HCF	heart:	n/a
17	chr19:18682484-18682534	AG04450	lung:	fetal
18	chr19:18682480-18682530	SKMC	muscle:	n/a
19	chr19:18682480-18682530	PFSK-1	brain:	n/a
20	chr19:18682463-18682513	SK-N-SH	brain:	n/a
21	chr19:18682480-18682530	HRCEpiC	kidney:	n/a
22	chr19:18682463-18682513	SK-N-MC	brain:	n/a
23	chr19:18682480-18682530	NB4	blood:	n/a
24	chr19:18682480-18682530	U87	brain:	n/a
25	chr19:18682484-18682534	ovcar-3	ovarian:	n/a
26	chr19:18682480-18682530	SAEC	small airway:	n/a
27	chr19:18682484-18682534	GM06990	blood:	n/a
28	chr19:18682480-18682530	CMK	blood:	n/a
29	chr19:18682484-18682534	LNCaP	prostate:	n/a
30	chr19:18682480-18682530	NHDF-neo	bronchial:	n/a
31	chr19:18682480-18682530	AoSMC	blood vessel:	n/a
32	chr19:18682463-18682513	HEEpiC	esophagus:	n/a
33	chr19:18682480-18682530	HNPCEpiC	eye:	n/a
34	chr19:18682463-18682513	NHDF-neo	bronchial:	n/a
35	chr19:18682484-18682534	NH-A	brain:	n/a
36	chr19:18682463-18682513	HRPEpiC	eye:	n/a
37	chr19:18682480-18682530	ProgFib	skin:	n/a
38	chr19:18682463-18682513	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:18682480-18682530	AG09309	skin:	n/a
40	chr19:18682484-18682534	T-47D	breast:	n/a
41	chr19:18682484-18682534	AoSMC	blood vessel:	n/a
42	chr19:18682463-18682513	Caco-2	colon:	n/a
43	chr19:18682480-18682530	GM12878	blood:	n/a
44	chr19:18682480-18682530	Hela-S3	cervix:	n/a
45	chr19:18682463-18682513	MCF-7	breast:	n/a
46	chr19:18682484-18682534	BJ	skin:	n/a
47	chr19:18682484-18682534	HRCEpiC	kidney:	n/a
48	chr19:18682463-18682513	SAEC	small airway:	n/a
49	chr19:18682480-18682530	HCF	heart:	n/a
50	chr19:18682480-18682530	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18631257..18635225-chr19:18680941..18684038,5	MCF-7	breast:
2	chr19:18629832..18635572-chr19:18680910..18686315,11	K562	blood:
3	chr19:18548448..18551673-chr19:18681148..18684161,3	K562	blood:
4	chr19:18682380..18683130-chr3:130568935..130569637,2	NB4	blood:
5	chr19:18682401..18684687-chr19:18702171..18705609,4	MCF-7	breast:
6	chr19:18666965..18674770-chr19:18676405..18685095,25	K562	blood:
7	chr19:18678376..18688390-chr19:18697032..18707656,34	K562	blood:
8	chr19:18671310..18673503-chr19:18682435..18684299,2	MCF-7	breast:
9	chr19:18651498..18655648-chr19:18680777..18683781,5	MCF-7	breast:
10	chr19:18586402..18589298-chr19:18680966..18684505,3	K562	blood:
11	chr14:102552851..102553436-chr19:18682313..18682926,2	Hela-S3	cervix:
12	chr19:18653470..18656783-chr19:18680897..18684291,6	K562	blood:
13	chr19:18682493..18683007-chr7:23338336..23339311,2	NB4	blood:
14	chr19:18682067..18684109-chr19:19302288..19304450,2	K562	blood:
15	chr19:18681104..18684544-chr19:18745683..18749906,4	K562	blood:
16	chr19:18667097..18671007-chr19:18677068..18684435,17	K562	blood:
17	chr19:18666812..18670172-chr19:18680715..18684041,6	MCF-7	breast:
18	chr10:32344972..32345499-chr19:18682349..18683038,2	HCT-116	colon:
19	chr19:18628801..18634367-chr19:18680492..18684131,12	MCF-7	breast:
20	chr19:18629832..18634516-chr19:18680910..18685097,11	K562	blood:
21	chr19:18682468..18683106-chr2:88926672..88927600,2	Hela-S3	cervix:
22	chr19:18681312..18685117-chr19:18698049..18701447,5	MCF-7	breast:
23	chr19:18651038..18656783-chr19:18680897..18685521,14	K562	blood:

Variant related genes	Relation type
UBA52	TF binding region
ENSG00000268983	TF binding region
ENSG00000268983	CpG island
UBA52	CpG island
ENSG00000170759	Chromatin interaction
ENSG00000105700	Chromatin interaction
ENSG00000105701	Chromatin interaction
ENSG00000167487	Chromatin interaction
ENSG00000006016	Chromatin interaction
ENSG00000064489	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000268030	Chromatin interaction
ENSG00000213999	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000156928	Chromatin interaction
ENSG00000064490	Chromatin interaction
ENSG00000080824	Chromatin interaction
ENSG00000254901	Chromatin interaction
ENSG00000172071	Chromatin interaction
ENSG00000017260	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000234028	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10409392	0.86[CHB][hapmap];1.00[YRI][hapmap]
rs10425018	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1043192	0.81[JPT][hapmap]
rs11086114	0.86[ASN][1000 genomes]
rs11086116	0.80[ASN][1000 genomes]
rs11667551	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11672297	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12150991	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12608925	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12609505	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1468475	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1862645	0.82[JPT][hapmap]
rs2057649	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2058077	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2079015	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2079016	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2238650	0.82[JPT][hapmap]
rs2302055	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2314664	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2314665	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314666	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314667	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28451415	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28711754	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3170474	0.85[JPT][hapmap]
rs35867875	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35875334	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36050418	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3761032	0.81[JPT][hapmap]
rs3761034	0.88[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3761036	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3795028	1.00[YRI][hapmap]
rs3803917	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4629093	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4808137	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4808821	0.90[ASN][1000 genomes]
rs4808839	0.81[JPT][hapmap]
rs55724121	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55888366	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58782998	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59798925	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62137086	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6554	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs709679	0.81[JPT][hapmap]
rs7250192	0.81[JPT][hapmap]
rs7250623	0.90[JPT][hapmap]
rs7253088	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7254004	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7256319	0.85[JPT][hapmap]
rs7258480	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8109364	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs8110371	0.86[EUR][1000 genomes]
rs8110374	0.86[EUR][1000 genomes]
rs916791	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
7	nsv911283	chr19:18626732-18689830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv911284	chr19:18643036-18684216	Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers Strong transcription 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	36 gene(s)	inside rSNPs	diseases
10	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2283616	UBA52	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18679800-18682600	Weak transcription	Small Intestine	intestine
2	chr19:18680600-18682600	Weak transcription	Spleen	Spleen
3	chr19:18681800-18682600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:18681800-18683200	Active TSS	Colonic Mucosa	Colon
5	chr19:18681800-18683200	Active TSS	Stomach Smooth Muscle	stomach
6	chr19:18681800-18683400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr19:18681800-18683400	Active TSS	Fetal Intestine Large	intestine
8	chr19:18681800-18683600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr19:18681800-18683600	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr19:18681800-18683600	Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr19:18681800-18683600	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr19:18682000-18682800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr19:18682000-18682800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
14	chr19:18682000-18682800	Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr19:18682000-18683000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr19:18682000-18683000	Active TSS	Brain Angular Gyrus	brain
17	chr19:18682000-18683200	Active TSS	Primary T cells from cord blood	blood
18	chr19:18682000-18683200	Active TSS	Brain Anterior Caudate	brain
19	chr19:18682000-18683200	Active TSS	Brain Cingulate Gyrus	brain
20	chr19:18682000-18683200	Active TSS	Brain Germinal Matrix	brain
21	chr19:18682000-18683200	Active TSS	Brain Hippocampus Middle	brain
22	chr19:18682000-18683200	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr19:18682000-18683200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr19:18682000-18683200	Active TSS	Brain Substantia Nigra	brain
25	chr19:18682000-18683200	Active TSS	Colon Smooth Muscle	Colon
26	chr19:18682000-18683200	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr19:18682000-18683200	Active TSS	Fetal Brain Male	brain
28	chr19:18682000-18683200	Active TSS	Fetal Stomach	stomach
29	chr19:18682000-18683200	Active TSS	Pancreas	Pancrea
30	chr19:18682000-18683200	Active TSS	Rectal Smooth Muscle	rectum
31	chr19:18682000-18683400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:18682000-18683400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr19:18682000-18683400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr19:18682000-18683400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr19:18682000-18683400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr19:18682000-18683400	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr19:18682000-18683400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:18682000-18683400	Active TSS	Fetal Brain Female	brain
39	chr19:18682000-18683400	Active TSS	Fetal Kidney	kidney
40	chr19:18682000-18683400	Active TSS	Fetal Lung	lung
41	chr19:18682000-18683400	Active TSS	Left Ventricle	heart
42	chr19:18682000-18683400	Active TSS	Right Atrium	heart
43	chr19:18682000-18683400	Active TSS	Right Ventricle	heart
44	chr19:18682000-18683400	Active TSS	NHDF-Ad	bronchial
45	chr19:18682000-18683600	Active TSS	H1 Cell Line	embryonic stem cell
46	chr19:18682000-18683600	Active TSS	H9 Cell Line	embryonic stem cell
47	chr19:18682000-18683600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr19:18682000-18683600	Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr19:18682000-18683600	Active TSS	Muscle Satellite Cultured Cells	--
50	chr19:18682000-18683600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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