Variant report

Variant	rs12611045
Chromosome Location	chr19:41119273-41119274
allele	C/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	MTA3	chr19:41119128-41120954	GM12878	blood:	n/a	n/a
2	POLR2A	chr19:41119238-41120019	GM12891	blood:	n/a	n/a
3	POLR2A	chr19:41119016-41120123	GM12878	blood:	n/a	n/a
4	E2F6	chr19:41119204-41120106	H1-hESC	embryonic stem cell:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
5	SP1	chr19:41118953-41120109	GM12878	blood:	n/a	chr19:41119593-41119602 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41119228-41119237 chr19:41120055-41120066 chr19:41119591-41119603 chr19:41119223-41119237 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119228-41119237 chr19:41119951-41119963 chr19:41118956-41118965 chr19:41119754-41119764 chr19:41119226-41119238 chr19:41119953-41119962 chr19:41119173-41119187 chr19:41119672-41119681 chr19:41118954-41118966 chr19:41119951-41119963 chr19:41119227-41119236 chr19:41120019-41120030 chr19:41119226-41119238 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41118955-41118965 chr19:41119588-41119602 chr19:41119227-41119237 chr19:41119227-41119237 chr19:41119246-41119258 chr19:41118955-41118969 chr19:41120035-41120046 chr19:41119591-41119603 chr19:41119592-41119602
6	POLR2A	chr19:41119199-41119576	A549	lung:	n/a	n/a
7	ETS1	chr19:41119105-41119690	A549	lung:	n/a	chr19:41119590-41119601 chr19:41119669-41119680 chr19:41119225-41119236
8	RCOR1	chr19:41119167-41120184	K562	blood:	n/a	n/a
9	HCFC1	chr19:41119182-41119913	K562	blood:	n/a	n/a
10	POLR2A	chr19:41118763-41120672	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr19:41119032-41119886	A549	lung:	n/a	chr19:41119190-41119198
12	USF2	chr19:41119120-41119403	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr19:41119223-41120081	GM12878	blood:	n/a	n/a
14	POLR2A	chr19:41119135-41119604	GM12878	blood:	n/a	n/a
15	E2F6	chr19:41119198-41120097	K562	blood:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
16	POLR2A	chr19:41118887-41120030	A549	lung:	n/a	n/a
17	POLR2A	chr19:41119198-41119481	GM12878	blood:	n/a	n/a
18	MAX	chr19:41119111-41120261	A549	lung:	n/a	chr19:41119225-41119235
19	SP1	chr19:41119166-41120109	A549	lung:	n/a	chr19:41119593-41119602 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41119228-41119237 chr19:41120055-41120066 chr19:41119591-41119603 chr19:41119223-41119237 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119228-41119237 chr19:41119951-41119963 chr19:41119754-41119764 chr19:41119226-41119238 chr19:41119953-41119962 chr19:41119173-41119187 chr19:41119672-41119681 chr19:41119951-41119963 chr19:41119227-41119236 chr19:41120019-41120030 chr19:41119226-41119238 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41119588-41119602 chr19:41119227-41119237 chr19:41119227-41119237 chr19:41119246-41119258 chr19:41120035-41120046 chr19:41119591-41119603 chr19:41119592-41119602
20	JUND	chr19:41119202-41119349	K562	blood:	n/a	n/a
21	POLR2A	chr19:41119006-41119549	H1-hESC	embryonic stem cell:	n/a	n/a
22	ZNF143	chr19:41119173-41120123	GM12878	blood:	n/a	n/a
23	GABPA	chr19:41118985-41119805	K562	blood:	n/a	chr19:41119227-41119236 chr19:41119592-41119601
24	STAT1	chr19:41119156-41120174	GM12878	blood:	n/a	chr19:41119493-41119505
25	ZBTB7A	chr19:41119109-41119514	K562	blood:	n/a	n/a
26	SP4	chr19:41118995-41119981	H1-hESC	embryonic stem cell:	n/a	chr19:41119244-41119260 chr19:41119589-41119605 chr19:41119224-41119240 chr19:41119587-41119603 chr19:41119751-41119767
27	SIN3A	chr19:41119010-41120846	H1-hESC	embryonic stem cell:	n/a	chr19:41119191-41119204 chr19:41120571-41120582
28	MAX	chr19:41119127-41120599	ECC-1	luminal epithelium:	n/a	chr19:41119225-41119235
29	EGR1	chr19:41119086-41119401	K562	blood:	n/a	chr19:41119222-41119235 chr19:41119225-41119235 chr19:41119242-41119255
30	E2F6	chr19:41119113-41120112	H1-hESC	embryonic stem cell:	n/a	chr19:41119592-41119601 chr19:41119227-41119236 chr19:41119779-41119790
31	BCL3	chr19:41119067-41119897	A549	lung:	n/a	chr19:41119190-41119198
32	POLR2A	chr19:41119175-41120130	GM19099	blood:	n/a	n/a
33	POLR2A	chr19:41118766-41120158	HCT-116	colon:	n/a	n/a
34	USF1	chr19:41119069-41119435	H1-hESC	embryonic stem cell:	n/a	n/a
35	GABPA	chr19:41119054-41119846	A549	lung:	n/a	chr19:41119227-41119236 chr19:41119592-41119601
36	CHD2	chr19:41119102-41119302	H1-hESC	embryonic stem cell:	n/a	n/a
37	USF2	chr19:41119165-41119455	GM12878	blood:	n/a	n/a
38	SIN3A	chr19:41119197-41119934	GM12878	blood:	n/a	n/a
39	EGR1	chr19:41119087-41119390	K562	blood:	n/a	chr19:41119222-41119235 chr19:41119225-41119235 chr19:41119242-41119255
40	TEAD4	chr19:41119153-41119976	K562	blood:	n/a	n/a
41	POLR2A	chr19:41119085-41120075	ECC-1	luminal epithelium:	n/a	n/a
42	RUNX3	chr19:41119193-41119585	GM12878	blood:	n/a	n/a
43	POLR2A	chr19:41119113-41119598	A549	lung:	n/a	n/a
44	SP1	chr19:41118911-41121215	H1-hESC	embryonic stem cell:	n/a	chr19:41119593-41119602 chr19:41120965-41120977 chr19:41119754-41119764 chr19:41119952-41119961 chr19:41119228-41119237 chr19:41120622-41120631 chr19:41120055-41120066 chr19:41120642-41120654 chr19:41120643-41120653 chr19:41119591-41119603 chr19:41119223-41119237 chr19:41119952-41119961 chr19:41119592-41119601 chr19:41119228-41119237 chr19:41119951-41119963 chr19:41118956-41118965 chr19:41119754-41119764 chr19:41119226-41119238 chr19:41120643-41120653 chr19:41119953-41119962 chr19:41119173-41119187 chr19:41119672-41119681 chr19:41118954-41118966 chr19:41120642-41120654 chr19:41119951-41119963 chr19:41120643-41120652 chr19:41119227-41119236 chr19:41120019-41120030 chr19:41119226-41119238 chr19:41119593-41119602 chr19:41119592-41119602 chr19:41120965-41120977 chr19:41118955-41118965 chr19:41120643-41120652 chr19:41119588-41119602 chr19:41120644-41120653 chr19:41120966-41120975 chr19:41119227-41119237 chr19:41119227-41119237 chr19:41119246-41119258 chr19:41118955-41118969 chr19:41120035-41120046 chr19:41121049-41121063 chr19:41119591-41119603 chr19:41119592-41119602 chr19:41120643-41120657
45	HEY1	chr19:41119206-41119479	K562	blood:	n/a	n/a
46	YY1	chr19:41119187-41119431	K562	blood:	n/a	chr19:41119227-41119236
47	TBP	chr19:41119169-41120025	GM12878	blood:	n/a	n/a
48	REST	chr19:41119131-41119448	A549	lung:	n/a	chr19:41119194-41119207 chr19:41119191-41119211
49	TAF1	chr19:41119019-41119369	H1-hESC	embryonic stem cell:	n/a	n/a
50	TAF1	chr19:41119139-41120107	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41076184..41077687-chr19:41117808..41119823,2	MCF-7	breast:
2	chr19:41118984..41122545-chr19:41130944..41134653,3	MCF-7	breast:
3	chr19:40971486..40973237-chr19:41118621..41121542,2	MCF-7	breast:
4	chr19:41119264..41121274-chr19:41121495..41123120,2	MCF-7	breast:
5	chr19:41119049..41119660-chr2:173940484..173941219,2	HCT-116	colon:
6	chr19:40948473..40950774-chr19:41118397..41120012,2	MCF-7	breast:
7	chr19:40971127..40973503-chr19:41117551..41119474,2	K562	blood:
8	chr19:41101978..41104325-chr19:41119218..41120800,2	MCF-7	breast:
9	chr19:41088760..41090446-chr19:41117467..41120079,2	K562	blood:
10	chr19:40789948..40791553-chr19:41119261..41121070,2	K562	blood:
11	chr19:40930456..40933734-chr19:41119113..41120830,3	K562	blood:
12	chr19:41117621..41122754-chr19:41128365..41133445,15	K562	blood:
13	chr19:40930456..40932097-chr19:41118468..41120699,2	K562	blood:

Variant related genes	Relation type
LTBP4	TF binding region
ENSG00000105221	Chromatin interaction
ENSG00000091436	Chromatin interaction
ENSG00000268366	Chromatin interaction
ENSG00000197019	Chromatin interaction
ENSG00000167565	Chromatin interaction
ENSG00000160460	Chromatin interaction
ENSG00000090006	Chromatin interaction
ENSG00000160410	Chromatin interaction
ENSG00000090013	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10402698	0.81[ASN][1000 genomes]
rs10403467	0.97[ASN][1000 genomes]
rs10403833	0.98[ASN][1000 genomes]
rs10403963	0.97[ASN][1000 genomes]
rs10405930	0.96[ASN][1000 genomes]
rs10410606	0.96[ASN][1000 genomes]
rs1051303	0.97[ASN][1000 genomes]
rs11083561	0.92[ASN][1000 genomes]
rs1131620	0.96[ASN][1000 genomes]
rs11667706	0.96[ASN][1000 genomes]
rs11667772	0.95[ASN][1000 genomes]
rs12980111	0.98[ASN][1000 genomes]
rs1318544	0.96[ASN][1000 genomes]
rs1864074	0.91[ASN][1000 genomes]
rs1864078	0.91[ASN][1000 genomes]
rs1869712	0.96[ASN][1000 genomes]
rs2278246	0.97[ASN][1000 genomes]
rs2303727	0.96[ASN][1000 genomes]
rs2303729	0.96[ASN][1000 genomes]
rs2369006	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2604902	0.96[ASN][1000 genomes]
rs28649715	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28655571	0.98[ASN][1000 genomes]
rs392726	0.85[ASN][1000 genomes]
rs393569	0.81[ASN][1000 genomes]
rs396118	0.85[ASN][1000 genomes]
rs404584	0.82[ASN][1000 genomes]
rs406133	0.80[ASN][1000 genomes]
rs415075	0.82[ASN][1000 genomes]
rs420720	0.84[ASN][1000 genomes]
rs4803348	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs56353506	0.98[ASN][1000 genomes]
rs7171	0.85[ASN][1000 genomes]
rs7259067	0.98[ASN][1000 genomes]
rs7259237	0.98[ASN][1000 genomes]
rs7259554	0.98[ASN][1000 genomes]
rs8107014	0.96[ASN][1000 genomes]
rs919307	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1830682	chr19:40880127-41270055	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv911714	chr19:41006426-41165252	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv911715	chr19:41014922-41141434	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers 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	33 gene(s)	inside rSNPs	diseases
4	nsv1057634	chr19:41019512-41174259	Enhancers Active TSS Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv911717	chr19:41023511-41141434	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS 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	33 gene(s)	inside rSNPs	diseases
6	nsv911719	chr19:41033109-41147087	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv911720	chr19:41033109-41156940	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	nsv911721	chr19:41040334-41124931	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription 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	33 gene(s)	inside rSNPs	diseases
9	nsv911722	chr19:41040334-41176403	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv911723	chr19:41075990-41195279	Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
11	nsv869561	chr19:41077513-41139834	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	nsv1064699	chr19:41086506-41174259	Genic enhancers Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
13	nsv911724	chr19:41089505-41165252	Bivalent/Poised TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
14	nsv911726	chr19:41090190-41141434	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
15	nsv911727	chr19:41111069-41200511	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
16	nsv911728	chr19:41111069-41211056	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
17	nsv870022	chr19:41113071-41178982	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41106000-41136800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:41109800-41122600	Weak transcription	Aorta	Aorta
3	chr19:41114400-41119400	Weak transcription	Ovary	ovary
4	chr19:41116400-41120000	Enhancers	Stomach Mucosa	stomach
5	chr19:41116600-41119400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr19:41116600-41119400	Weak transcription	Right Atrium	heart
7	chr19:41116600-41119800	Weak transcription	NHLF	lung
8	chr19:41116600-41137000	Weak transcription	Psoas Muscle	Psoas
9	chr19:41117000-41119400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr19:41117000-41119400	Weak transcription	NHDF-Ad	bronchial
11	chr19:41117000-41119800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr19:41117000-41121800	Weak transcription	Hela-S3	cervix
13	chr19:41117000-41140200	Weak transcription	Brain Angular Gyrus	brain
14	chr19:41117200-41119600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr19:41117200-41120400	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr19:41117400-41119400	Weak transcription	Brain Hippocampus Middle	brain
17	chr19:41117400-41119400	Weak transcription	Brain Substantia Nigra	brain
18	chr19:41117400-41125200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr19:41118200-41119400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr19:41118200-41119400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr19:41118400-41120400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
22	chr19:41118800-41119800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:41118800-41120600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr19:41118800-41121200	Active TSS	H9 Cell Line	embryonic stem cell
25	chr19:41118800-41121400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:41119000-41119400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr19:41119000-41119400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
28	chr19:41119000-41119400	Enhancers	Gastric	stomach
29	chr19:41119000-41119400	Enhancers	Lung	lung
30	chr19:41119000-41119600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr19:41119000-41119800	Flanking Active TSS	Colonic Mucosa	Colon
32	chr19:41119000-41119800	Flanking Active TSS	K562	blood
33	chr19:41119000-41120000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr19:41119000-41120400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:41119000-41120600	Active TSS	Osteobl	bone
36	chr19:41119000-41121000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr19:41119000-41121000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr19:41119000-41121000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr19:41119000-41121000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
40	chr19:41119000-41121200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr19:41119000-41121200	Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr19:41119000-41121200	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr19:41119000-41121200	Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr19:41119000-41121200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
45	chr19:41119000-41121400	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr19:41119000-41121400	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr19:41119000-41121400	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr19:41119000-41121400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr19:41119000-41121400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr19:41119200-41119400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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