Variant report

Variant	rs7248540
Chromosome Location	chr19:38877923-38877924
allele	A/G
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	NR2F2	chr19:38877744-38878688	K562	blood:	n/a	n/a
2	GABPA	chr19:38877876-38878250	H1-hESC	embryonic stem cell:	n/a	n/a
3	ZMIZ1	chr19:38877893-38878145	K562	blood:	n/a	n/a
4	POLR2A	chr19:38877527-38877924	ECC-1	luminal epithelium:	n/a	n/a
5	POLR2A	chr19:38871440-38886227	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr19:38877152-38881859	PFSK-1	brain:	n/a	n/a
7	POLR2A	chr19:38874785-38879102	A549	lung:	n/a	n/a
8	TEAD4	chr19:38877868-38878235	K562	blood:	n/a	n/a
9	SPI1	chr19:38877794-38877935	K562	blood:	n/a	n/a
10	POLR2A	chr19:38869603-38879135	K562	blood:	n/a	n/a
11	TCF12	chr19:38877896-38880448	A549	lung:	n/a	chr19:38878480-38878487
12	TEAD4	chr19:38877808-38878551	K562	blood:	n/a	n/a
13	POLR2A	chr19:38877558-38878783	ECC-1	luminal epithelium:	n/a	n/a
14	MAZ	chr19:38877673-38879268	K562	blood:	n/a	chr19:38878570-38878580 chr19:38878754-38878763 chr19:38878750-38878760
15	POLR2A	chr19:38877745-38879927	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr19:38877882-38878119	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr19:38877745-38877959	HepG2	liver:	n/a	n/a
18	POLR2A	chr19:38877536-38878371	GM12892	blood:	n/a	n/a
19	POLR2A	chr19:38877808-38879269	U87	brain:	n/a	n/a
20	POLR2A	chr19:38873453-38879163	K562	blood:	n/a	n/a
21	ZBTB7A	chr19:38877661-38879283	K562	blood:	n/a	chr19:38878920-38878927
22	SIN3AK20	chr19:38877902-38878564	A549	lung:	n/a	n/a
23	POLR2A	chr19:38873627-38879112	K562	blood:	n/a	n/a
24	POLR2A	chr19:38877611-38878665	GM12878	blood:	n/a	n/a
25	BHLHE40	chr19:38877875-38878197	K562	blood:	n/a	chr19:38878001-38878017
26	RCOR1	chr19:38877892-38878780	K562	blood:	n/a	n/a
27	HMGN3	chr19:38877286-38878075	K562	blood:	n/a	n/a
28	MAX	chr19:38877849-38878491	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr19:38877802-38879275	U87	brain:	n/a	n/a
30	SP1	chr19:38877908-38879494	A549	lung:	n/a	chr19:38879469-38879478 chr19:38878247-38878259 chr19:38878009-38878019 chr19:38878549-38878558 chr19:38878549-38878559 chr19:38878803-38878815 chr19:38879464-38879478 chr19:38878804-38878813 chr19:38878571-38878580 chr19:38879019-38879029 chr19:38878915-38878927 chr19:38878010-38878019 chr19:38878247-38878259 chr19:38878750-38878760 chr19:38878704-38878716 chr19:38878989-38878999 chr19:38878803-38878815 chr19:38878222-38878231 chr19:38878009-38878018 chr19:38878676-38878687 chr19:38879467-38879479 chr19:38878915-38878927 chr19:38878569-38878581 chr19:38878704-38878716 chr19:38878704-38878715 chr19:38878570-38878579 chr19:38878723-38878732 chr19:38878804-38878814 chr19:38878749-38878761 chr19:38878705-38878719 chr19:38878750-38878760 chr19:38878569-38878581 chr19:38879018-38879030 chr19:38878548-38878560 chr19:38879018-38879030 chr19:38878804-38878818 chr19:38878749-38878761 chr19:38878804-38878814 chr19:38878550-38878559 chr19:38878009-38878018 chr19:38878008-38878020 chr19:38879102-38879111 chr19:38878722-38878733 chr19:38879468-38879477 chr19:38878549-38878559 chr19:38878706-38878715 chr19:38878549-38878558 chr19:38878570-38878584 chr19:38878916-38878925 chr19:38878570-38878580 chr19:38879467-38879479 chr19:38878248-38878262 chr19:38878705-38878714 chr19:38878750-38878759 chr19:38878805-38878814 chr19:38878008-38878020 chr19:38878804-38878813 chr19:38878009-38878019 chr19:38879468-38879478 chr19:38878751-38878760 chr19:38879019-38879028 chr19:38878548-38878560
31	RCOR1	chr19:38877836-38878525	K562	blood:	n/a	n/a
32	CCNT2	chr19:38876270-38877985	K562	blood:	n/a	n/a
33	MYC	chr19:38877726-38878800	K562	blood:	n/a	chr19:38878570-38878580 chr19:38878754-38878763 chr19:38878750-38878760
34	POLR2A	chr19:38877921-38880619	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr19:38877356-38877962	HL-60	blood:	n/a	n/a
36	NR2F2	chr19:38877836-38878269	K562	blood:	n/a	n/a
37	PBX3	chr19:38877834-38879471	SK-N-SH	brain:	n/a	n/a
38	POLR2A	chr19:38877896-38877949	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr19:38877642-38879268	PANC-1	pancreas:	n/a	n/a
40	UBTF	chr19:38877865-38878613	K562	blood:	n/a	n/a
41	MAX	chr19:38877558-38878733	K562	blood:	n/a	chr19:38878570-38878580
42	POLR2A	chr19:38877691-38879188	A549	lung:	n/a	n/a
43	MAZ	chr19:38877571-38881281	IMR90	lung:	n/a	chr19:38879857-38879866 chr19:38879857-38879866 chr19:38878570-38878580 chr19:38879857-38879866 chr19:38878754-38878763 chr19:38879466-38879476 chr19:38878750-38878760
44	BCL3	chr19:38877853-38879450	A549	lung:	n/a	n/a
45	POLR2A	chr19:38877651-38877988	GM12892	blood:	n/a	n/a
46	POLR2A	chr19:38877669-38877923	ProgFib	skin:	n/a	n/a
47	IRF1	chr19:38877863-38879226	K562	blood:	n/a	chr19:38879016-38879030 chr19:38878546-38878560 chr19:38878747-38878761 chr19:38878006-38878020 chr19:38878567-38878581 chr19:38878245-38878259 chr19:38878913-38878927 chr19:38878801-38878815
48	POLR2A	chr19:38877103-38879265	PANC-1	pancreas:	n/a	n/a
49	BCL3	chr19:38877842-38879405	A549	lung:	n/a	n/a
50	UBTF	chr19:38877793-38878145	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:38877874-38877924	AG04449	skin:	fetal
2	chr19:38877874-38877924	IMR90	lung:	fetal
3	chr19:38877874-38877924	MCF-7	breast:	n/a
4	chr19:38877874-38877924	HUVEC	blood vessel:	n/a
5	chr19:38877874-38877924	A549	lung:	n/a
6	chr19:38877874-38877924	LNCaP	prostate:	n/a
7	chr19:38877874-38877924	GM12878	blood:	n/a
8	chr19:38877874-38877924	HCT-116	colon:	n/a
9	chr19:38877874-38877924	PFSK-1	brain:	n/a
10	chr19:38877874-38877924	AG04450	lung:	fetal
11	chr19:38877874-38877924	HPAEpiC	pulmonary alveolar:	n/a
12	chr19:38877874-38877924	SK-N-MC	brain:	n/a
13	chr19:38877874-38877924	HRE	kidney:	n/a
14	chr19:38877874-38877924	Hela-S3	cervix:	n/a
15	chr19:38877874-38877924	HAEpiC	amniotic membrane:	n/a
16	chr19:38877874-38877924	ovcar-3	ovarian:	n/a
17	chr19:38877874-38877924	K562	blood:	n/a
18	chr19:38877874-38877924	GM06990	blood:	n/a
19	chr19:38877874-38877924	HRCEpiC	kidney:	n/a
20	chr19:38877874-38877924	NH-A	brain:	n/a
21	chr19:38877874-38877924	AG09309	skin:	n/a
22	chr19:38877874-38877924	NB4	blood:	n/a
23	chr19:38877874-38877924	RPTEC	kidney:	n/a
24	chr19:38877874-38877924	HIPEpiC	eye:	n/a
25	chr19:38877874-38877924	GM12892	blood:	n/a
26	chr19:38877874-38877924	CMK	blood:	n/a
27	chr19:38877874-38877924	HRPEpiC	eye:	n/a
28	chr19:38877874-38877924	HMEC	breast:	n/a
29	chr19:38877874-38877924	H1-hESC	embryonic stem cell:	embryo
30	chr19:38877874-38877924	SK-N-SH	brain:	n/a
31	chr19:38877874-38877924	Hepatocyte	liver:	n/a
32	chr19:38877874-38877924	ECC-1	luminal epithelium:	n/a
33	chr19:38877874-38877924	U87	brain:	n/a
34	chr19:38877874-38877924	PANC-1	pancreas:	n/a
35	chr19:38877874-38877924	NT2-D1	testis:	n/a
36	chr19:38877874-38877924	NHDF-neo	bronchial:	n/a
37	chr19:38877874-38877924	BJ	skin:	n/a
38	chr19:38877874-38877924	BE2_C	brain:	n/a
39	chr19:38877874-38877924	GM12891	blood:	n/a
40	chr19:38877874-38877924	HNPCEpiC	eye:	n/a
41	chr19:38877874-38877924	PrEC	prostate:	n/a
42	chr19:38877874-38877924	SAEC	small airway:	n/a
43	chr19:38877874-38877924	Caco-2	colon:	n/a
44	chr19:38877874-38877924	HCF	heart:	n/a
45	chr19:38877874-38877924	Jurkat	blood:	n/a
46	chr19:38877874-38877924	T-47D	breast:	n/a
47	chr19:38877874-38877924	HL-60	blood:	n/a
48	chr19:38877874-38877924	AG09319	gingival:	n/a
49	chr19:38877874-38877924	HEEpiC	esophagus:	n/a
50	chr19:38877874-38877924	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:38876175..38878484-chr19:38901904..38903905,2	K562	blood:
2	chr19:38851103..38853998-chr19:38877778..38880419,3	K562	blood:
3	chr19:38873942..38878444-chr19:38892255..38895006,5	K562	blood:
4	chr19:38805296..38807779-chr19:38877097..38880049,2	K562	blood:
5	chr19:36630602..36632414-chr19:38875371..38878496,3	MCF-7	breast:
6	chr19:38851827..38854715-chr19:38877414..38880419,4	K562	blood:
7	chr19:38717810..38720228-chr19:38876711..38878921,2	K562	blood:
8	chr19:38724122..38725097-chr19:38877454..38878445,2	K562	blood:
9	chr19:38851829..38853788-chr19:38876902..38878905,2	MCF-7	breast:
10	chr19:38824957..38829265-chr19:38874295..38879043,8	MCF-7	breast:
11	chr19:38825387..38828116-chr19:38877119..38879831,3	MCF-7	breast:

Variant related genes	Relation type
SPRED3	TF binding region
SPRED3	CpG island
ENSG00000126247	Chromatin interaction
ENSG00000167645	Chromatin interaction
ENSG00000130244	Chromatin interaction
ENSG00000099338	Chromatin interaction
ENSG00000011332	Chromatin interaction
ENSG00000171777	Chromatin interaction
ENSG00000266963	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10993	1.00[CEU][hapmap]
rs11083454	1.00[ASW][hapmap];0.82[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11538289	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11880301	1.00[CEU][hapmap]
rs2074981	0.81[TSI][hapmap]
rs2302228	1.00[EUR][1000 genomes]
rs3745955	0.80[EUR][1000 genomes]
rs3745963	1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3760884	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3786874	0.81[TSI][hapmap]
rs57753437	0.93[EUR][1000 genomes]
rs59491640	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60780508	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6508791	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6508792	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6508793	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7245668	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7246085	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7246191	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7246213	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7248780	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7257976	1.00[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73043029	0.81[EUR][1000 genomes]
rs73043030	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs73043033	0.93[EUR][1000 genomes]
rs73043098	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73044905	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044908	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044911	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044915	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044917	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044919	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044923	0.80[EUR][1000 genomes]
rs73044926	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044928	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044930	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044932	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044937	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044944	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044947	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044948	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73044953	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8108440	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8109713	1.00[CEU][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8112499	1.00[CEU][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063471	chr19:38734744-39148392	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
2	nsv833822	chr19:38760748-38945105	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
3	nsv911658	chr19:38785318-39002140	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
4	nsv470140	chr19:38840139-39119494	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS 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	43 gene(s)	inside rSNPs	diseases
5	nsv911659	chr19:38852357-39002140	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
6	nsv911660	chr19:38852357-39060238	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv833823	chr19:38855550-39035800	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1064275	chr19:38859865-38913251	Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv911661	chr19:38872335-38894829	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	nsv911662	chr19:38872634-38895809	Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
11	esv1803709	chr19:38874828-38900078	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38867000-38878000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr19:38874800-38878000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr19:38874800-38878000	Weak transcription	HepG2	liver
4	chr19:38874800-38878200	Weak transcription	HSMMtube	muscle
5	chr19:38875000-38878000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr19:38875200-38878400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr19:38875200-38878400	Weak transcription	Aorta	Aorta
8	chr19:38875800-38878000	Weak transcription	Brain Angular Gyrus	brain
9	chr19:38875800-38878200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr19:38876200-38878000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr19:38876200-38878000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr19:38876200-38880200	Enhancers	Fetal Heart	heart
13	chr19:38876400-38878000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:38876400-38880600	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr19:38876600-38878200	Bivalent Enhancer	Fetal Stomach	stomach
16	chr19:38876600-38878600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr19:38876600-38879200	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
18	chr19:38876800-38878000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
19	chr19:38876800-38878000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
20	chr19:38876800-38878000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr19:38876800-38878000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
22	chr19:38876800-38878200	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr19:38876800-38878400	Bivalent Enhancer	Fetal Thymus	thymus
24	chr19:38876800-38879000	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr19:38876800-38879200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr19:38876800-38880200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr19:38876800-38881400	Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr19:38877000-38878000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
29	chr19:38877000-38878000	Enhancers	Placenta	Placenta
30	chr19:38877000-38878000	Enhancers	Ovary	ovary
31	chr19:38877000-38878000	Enhancers	Pancreas	Pancrea
32	chr19:38877000-38878200	Enhancers	Right Ventricle	heart
33	chr19:38877000-38878200	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr19:38877000-38879400	Enhancers	Lung	lung
35	chr19:38877200-38878000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr19:38877200-38878000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr19:38877200-38878000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr19:38877200-38878000	Enhancers	NHDF-Ad	bronchial
39	chr19:38877200-38878200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr19:38877200-38878200	Enhancers	Left Ventricle	heart
41	chr19:38877200-38878200	Enhancers	NH-A	brain
42	chr19:38877200-38879200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
43	chr19:38877200-38880200	Flanking Active TSS	Dnd41	blood
44	chr19:38877400-38878000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr19:38877400-38878000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr19:38877400-38878000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr19:38877400-38878000	Bivalent Enhancer	Fetal Brain Male	brain
48	chr19:38877400-38878200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr19:38877400-38878200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr19:38877400-38878200	Enhancers	Psoas Muscle	Psoas

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