Variant report

Variant	rs545339680
Chromosome Location	chr19:18528019-18528020
allele	C/T
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	chr19:18527098-18529165	MCF-7	breast:	n/a	chr19:18527972-18527979 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980 chr19:18528686-18528696
2	POLR2A	chr19:18527106-18528760	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr19:18527862-18528582	GM12892	blood:	n/a	n/a
4	UBTF	chr19:18527657-18528662	K562	blood:	n/a	n/a
5	POLR2A	chr19:18527049-18529017	K562	blood:	n/a	n/a
6	YY1	chr19:18527607-18528090	K562	blood:	n/a	n/a
7	EP300	chr19:18527618-18528178	A549	lung:	n/a	chr19:18527976-18527989 chr19:18527817-18527833 chr19:18527702-18527718
8	CREB1	chr19:18526983-18528154	H1-hESC	embryonic stem cell:	n/a	n/a
9	HMGN3	chr19:18527316-18528048	K562	blood:	n/a	n/a
10	SIN3A	chr19:18527700-18528230	GM12878	blood:	n/a	n/a
11	POLR2A	chr19:18527623-18528179	ProgFib	skin:	n/a	n/a
12	USF1	chr19:18527868-18528102	SK-N-SH_RA	brain:	n/a	n/a
13	POLR2A	chr19:18525610-18530298	SK-N-MC	brain:	n/a	n/a
14	ZBTB7A	chr19:18527543-18528967	K562	blood:	n/a	chr19:18528162-18528171 chr19:18528520-18528527
15	POLR2A	chr19:18527095-18528938	K562	blood:	n/a	n/a
16	MAX	chr19:18526925-18531451	K562	blood:	n/a	chr19:18527972-18527979 chr19:18529211-18529221 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980 chr19:18528686-18528696 chr19:18529634-18529643
17	POLR2A	chr19:18527025-18528787	HCT-116	colon:	n/a	n/a
18	MAX	chr19:18526998-18529277	A549	lung:	n/a	chr19:18527972-18527979 chr19:18529211-18529221 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980 chr19:18528686-18528696
19	POLR2A	chr19:18527622-18528480	MCF-7	breast:	n/a	n/a
20	SIN3AK20	chr19:18527778-18528121	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr19:18527064-18528665	SK-N-MC	brain:	n/a	n/a
22	YY1	chr19:18527146-18528026	K562	blood:	n/a	n/a
23	POLR2A	chr19:18526995-18528898	HUVEC	blood vessel:	n/a	n/a
24	MAZ	chr19:18527615-18528793	HepG2	liver:	n/a	chr19:18527972-18527979 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980 chr19:18528686-18528696
25	POLR2A	chr19:18527518-18528728	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr19:18527532-18528740	U87	brain:	n/a	n/a
27	ZBTB7A	chr19:18527576-18528943	ECC-1	luminal epithelium:	n/a	chr19:18528162-18528171 chr19:18528520-18528527
28	ARID3A	chr19:18527122-18528092	K562	blood:	n/a	n/a
29	EGR1	chr19:18527244-18529118	K562	blood:	n/a	chr19:18528591-18528601 chr19:18528838-18528852 chr19:18528842-18528852 chr19:18528990-18529003 chr19:18528537-18528546 chr19:18528842-18528851 chr19:18528993-18529006 chr19:18528840-18528854 chr19:18527657-18527670 chr19:18528989-18528999 chr19:18528498-18528512 chr19:18528586-18528599 chr19:18528688-18528698 chr19:18528842-18528852 chr19:18528686-18528696 chr19:18528683-18528696
30	SIN3A	chr19:18527191-18528608	H1-hESC	embryonic stem cell:	n/a	chr19:18528334-18528347
31	MYC	chr19:18527031-18531008	K562	blood:	n/a	chr19:18527972-18527979 chr19:18529211-18529221 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980 chr19:18528686-18528696 chr19:18529634-18529643
32	POLR2A	chr19:18527226-18528921	U87	brain:	n/a	n/a
33	GTF2F1	chr19:18527142-18528469	K562	blood:	n/a	n/a
34	HA-E2F1	chr19:18527487-18528226	MCF-7	breast:	n/a	chr19:18527812-18527824 chr19:18527824-18527833 chr19:18527812-18527823
35	SMARCC1	chr19:18527164-18528528	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr19:18526951-18529116	K562	blood:	n/a	n/a
37	EBF1	chr19:18527599-18528105	GM12878	blood:	n/a	chr19:18527945-18527956
38	CHD1	chr19:18527959-18528144	GM12878	blood:	n/a	n/a
39	MYC	chr19:18527071-18528215	K562	blood:	n/a	chr19:18527972-18527979 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980
40	CTBP2	chr19:18527646-18528535	H1-hESC	embryonic stem cell:	n/a	n/a
41	BCLAF1	chr19:18528000-18528798	K562	blood:	n/a	chr19:18528537-18528546 chr19:18528689-18528698
42	POLR2A	chr19:18527066-18529321	HL-60	blood:	n/a	n/a
43	POLR2A	chr19:18527920-18528436	GM12878	blood:	n/a	n/a
44	POLR2A	chr19:18527337-18528582	Gliobla	brain:	n/a	n/a
45	POLR2A	chr19:18527039-18528371	K562	blood:	n/a	n/a
46	CHD2	chr19:18527176-18528519	H1-hESC	embryonic stem cell:	n/a	n/a
47	RCOR1	chr19:18527107-18528681	K562	blood:	n/a	n/a
48	EBF1	chr19:18527790-18528029	GM12878	blood:	n/a	chr19:18527945-18527956
49	POLR2A	chr19:18527111-18531151	Hela-S3	cervix:	n/a	n/a
50	MYC	chr19:18527715-18528177	HUVEC	blood vessel:	n/a	chr19:18527972-18527979 chr19:18527789-18527798 chr19:18527971-18527980 chr19:18527971-18527980

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18527971-18528021	Hela-S3	cervix:	n/a
2	chr19:18527971-18528021	ProgFib	skin:	n/a
3	chr19:18527971-18528021	AG04449	skin:	fetal
4	chr19:18527971-18528021	CMK	blood:	n/a
5	chr19:18527971-18528021	A549	lung:	n/a
6	chr19:18527971-18528021	NHDF-neo	bronchial:	n/a
7	chr19:18527971-18528021	BE2_C	brain:	n/a
8	chr19:18527971-18528021	NT2-D1	testis:	n/a
9	chr19:18527971-18528021	SK-N-SH	brain:	n/a
10	chr19:18527971-18528021	HepG2	liver:	n/a
11	chr19:18527971-18528021	SKMC	muscle:	n/a
12	chr19:18527971-18528021	HRE	kidney:	n/a
13	chr19:18527971-18528021	SK-N-MC	brain:	n/a
14	chr19:18527971-18528021	HEEpiC	esophagus:	n/a
15	chr19:18527971-18528021	AG10803	skin:	n/a
16	chr19:18527971-18528021	HPAEpiC	pulmonary alveolar:	n/a
17	chr19:18527971-18528021	AG09309	skin:	n/a
18	chr19:18527971-18528021	NB4	blood:	n/a
19	chr19:18527971-18528021	AG09319	gingival:	n/a
20	chr19:18527971-18528021	PANC-1	pancreas:	n/a
21	chr19:18527971-18528021	LNCaP	prostate:	n/a
22	chr19:18527971-18528021	RPTEC	kidney:	n/a
23	chr19:18527971-18528021	HNPCEpiC	eye:	n/a
24	chr19:18527971-18528021	K562	blood:	n/a
25	chr19:18527971-18528021	SAEC	small airway:	n/a
26	chr19:18527971-18528021	PFSK-1	brain:	n/a
27	chr19:18527971-18528021	HUVEC	blood vessel:	n/a
28	chr19:18527971-18528021	HRCEpiC	kidney:	n/a
29	chr19:18527971-18528021	HRPEpiC	eye:	n/a
30	chr19:18527971-18528021	Jurkat	blood:	n/a
31	chr19:18527971-18528021	HAEpiC	amniotic membrane:	n/a
32	chr19:18527971-18528021	T-47D	breast:	n/a
33	chr19:18527971-18528021	HL-60	blood:	n/a
34	chr19:18527971-18528021	MCF-7	breast:	n/a
35	chr19:18527971-18528021	H1-hESC	embryonic stem cell:	embryo
36	chr19:18527971-18528021	HMEC	breast:	n/a
37	chr19:18527971-18528021	ECC-1	luminal epithelium:	n/a
38	chr19:18527971-18528021	HCT-116	colon:	n/a
39	chr19:18527971-18528021	NH-A	brain:	n/a
40	chr19:18527971-18528021	U87	brain:	n/a
41	chr19:18527971-18528021	HCF	heart:	n/a
42	chr19:18527971-18528021	IMR90	lung:	fetal
43	chr19:18527971-18528021	Hepatocyte	liver:	n/a
44	chr19:18527971-18528021	BJ	skin:	n/a
45	chr19:18527971-18528021	GM12891	blood:	n/a
46	chr19:18527971-18528021	GM19239	blood:	n/a
47	chr19:18527971-18528021	HCPEpiC	choroid plexus:	n/a
48	chr19:18527971-18528021	PrEC	prostate:	n/a
49	chr19:18527971-18528021	Caco-2	colon:	n/a
50	chr19:18527971-18528021	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18385043..18394940-chr19:18518893..18533267,53	K562	blood:
2	chr19:18333703..18336599-chr19:18524425..18529905,5	K562	blood:
3	chr19:18515749..18518459-chr19:18525942..18528660,2	K562	blood:
4	chr19:18520199..18523408-chr19:18523976..18531789,10	MCF-7	breast:
5	chr19:18496334..18499990-chr19:18526862..18529675,5	MCF-7	breast:
6	chr19:18495547..18503463-chr19:18525062..18531964,43	K562	blood:
7	chr19:18333200..18334741-chr19:18526229..18528340,2	K562	blood:
8	chr19:18483533..18485446-chr19:18527365..18529374,2	K562	blood:
9	chr19:18421126..18423149-chr19:18527568..18529347,2	MCF-7	breast:
10	chr16:69165652..69166579-chr19:18527926..18528518,2	Hela-S3	cervix:
11	chr19:18527987..18529989-chr19:18630753..18632961,2	K562	blood:
12	chr19:18521178..18523940-chr19:18526171..18529152,3	MCF-7	breast:
13	chr19:18265654..18267596-chr19:18526831..18528675,2	K562	blood:
14	chr19:18399894..18406849-chr19:18524216..18528146,7	K562	blood:
15	chr19:18527544..18530023-chr19:18699407..18700970,2	K562	blood:
16	chr19:18508054..18515743-chr19:18523957..18529414,9	K562	blood:
17	chr19:18527431..18533703-chr19:18536573..18544512,11	MCF-7	breast:
18	chr19:18448952..18453435-chr19:18523841..18530143,7	K562	blood:
19	chr19:18388809..18393836-chr19:18524501..18532718,14	MCF-7	breast:
20	chr19:18383371..18384902-chr19:18527058..18529406,2	K562	blood:
21	chr19:18527420..18529466-chr19:49466752..49468633,2	K562	blood:
22	chr19:18474455..18476591-chr19:18526226..18528576,3	K562	blood:
23	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
24	chr19:18527888..18529469-chr19:18682713..18684941,2	K562	blood:
25	chr19:18526729..18529360-chr19:19028525..19030689,2	MCF-7	breast:
26	chr12:49760185..49761113-chr19:18527723..18528583,2	Hela-S3	cervix:
27	chr19:18391038..18394210-chr19:18525828..18530797,8	MCF-7	breast:
28	chr19:18263382..18266326-chr19:18527834..18529427,2	K562	blood:
29	chr19:18526882..18530762-chr19:18548138..18550714,4	MCF-7	breast:
30	chr19:18334858..18337739-chr19:18526520..18530329,6	K562	blood:
31	chr19:18472311..18474156-chr19:18526952..18528977,3	K562	blood:
32	chr19:18312986..18316928-chr19:18526182..18529449,5	K562	blood:

Variant related genes	Relation type
SSBP4	TF binding region
SSBP4	CpG island
ENSG00000105647	Chromatin interaction
ENSG00000268650	Chromatin interaction
ENSG00000221167	Chromatin interaction
ENSG00000087086	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000123352	Chromatin interaction
ENSG00000105671	Chromatin interaction
ENSG00000168802	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000141076	Chromatin interaction
ENSG00000268173	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000241464	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000105649	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000267898	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000175489	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000221983	Chromatin interaction
ENSG00000105669	Chromatin interaction
ENSG00000105650	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000130517	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription 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	167 gene(s)	inside rSNPs	diseases
3	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
8	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
9	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
10	nsv911277	chr19:18520231-18552139	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
11	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
12	nsv911278	chr19:18526536-18550276	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 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	chr19:18525000-18529600	Enhancers	Liver	Liver
2	chr19:18525000-18529600	Enhancers	Spleen	Spleen
3	chr19:18525200-18529600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr19:18525400-18529600	Enhancers	Lung	lung
5	chr19:18526200-18528400	Flanking Active TSS	Fetal Lung	lung
6	chr19:18526400-18528800	Active TSS	Ovary	ovary
7	chr19:18526800-18528200	Bivalent Enhancer	Fetal Thymus	thymus
8	chr19:18527200-18528200	Active TSS	iPS-18 Cell Line	embryonic stem cell
9	chr19:18527200-18528400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:18527200-18528400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr19:18527200-18528400	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr19:18527200-18528400	Flanking Active TSS	Fetal Muscle Leg	muscle
13	chr19:18527200-18528600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr19:18527200-18528600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
15	chr19:18527200-18528600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
16	chr19:18527200-18528600	Flanking Bivalent TSS/Enh	Dnd41	blood
17	chr19:18527200-18529000	Flanking Active TSS	Osteobl	bone
18	chr19:18527200-18529200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr19:18527200-18530000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr19:18527200-18530000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr19:18527200-18530000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr19:18527200-18530200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr19:18527400-18528200	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr19:18527400-18528200	Flanking Active TSS	HMEC	breast
25	chr19:18527400-18528400	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr19:18527400-18528400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr19:18527400-18528400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr19:18527400-18528400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:18527400-18528400	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr19:18527400-18528400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr19:18527400-18528400	Flanking Active TSS	Placenta	Placenta
32	chr19:18527400-18528400	Flanking Active TSS	Fetal Stomach	stomach
33	chr19:18527400-18528400	Flanking Active TSS	HepG2	liver
34	chr19:18527400-18528600	Flanking Active TSS	NHEK	skin
35	chr19:18527400-18528800	Active TSS	H9 Cell Line	embryonic stem cell
36	chr19:18527400-18528800	Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr19:18527400-18528800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
38	chr19:18527400-18529000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr19:18527400-18529000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr19:18527400-18529000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr19:18527400-18529000	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
42	chr19:18527400-18529000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr19:18527400-18529200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr19:18527400-18529200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr19:18527400-18529400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
46	chr19:18527400-18529800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
47	chr19:18527400-18530000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr19:18527400-18530000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr19:18527400-18530000	Flanking Active TSS	Right Ventricle	heart
50	chr19:18527400-18530200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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