Variant report

Variant	rs533734
Chromosome Location	chr19:56612698-56612699
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:56612215-56612811	K562	blood:	n/a	n/a
2	POLR2A	chr19:56612257-56612731	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr19:56611900-56612728	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr19:56611302-56612865	GM12878	blood:	n/a	n/a
5	POLR2A	chr19:56611422-56612928	PANC-1	pancreas:	n/a	n/a
6	TCF3	chr19:56612474-56612767	GM12878	blood:	n/a	n/a
7	POLR2A	chr19:56612455-56613222	K562	blood:	n/a	n/a
8	POLR2A	chr19:56612665-56612785	K562	blood:	n/a	n/a
9	POLR2A	chr19:56611950-56612787	GM12878	blood:	n/a	n/a
10	POLR2A	chr19:56611124-56613783	HepG2	liver:	n/a	n/a
11	POLR2A	chr19:56611436-56612715	GM12891	blood:	n/a	n/a
12	POLR2A	chr19:56611283-56612868	GM12892	blood:	n/a	n/a
13	POLR2A	chr19:56611919-56612808	GM12878	blood:	n/a	n/a
14	POLR2A	chr19:56612010-56612802	GM12891	blood:	n/a	n/a
15	POLR2A	chr19:56611838-56612710	GM12891	blood:	n/a	n/a
16	POLR2A	chr19:56612299-56612703	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56612697-56612747	T-47D	breast:	n/a
2	chr19:56612697-56612747	SKMC	muscle:	n/a
3	chr19:56612697-56612747	NH-A	brain:	n/a
4	chr19:56612697-56612747	K562	blood:	n/a
5	chr19:56612697-56612747	HEEpiC	esophagus:	n/a
6	chr19:56612697-56612747	Hepatocyte	liver:	n/a
7	chr19:56612697-56612747	NHDF-neo	bronchial:	n/a
8	chr19:56612697-56612747	HUVEC	blood vessel:	n/a
9	chr19:56612697-56612747	HRE	kidney:	n/a
10	chr19:56612697-56612747	NT2-D1	testis:	n/a
11	chr19:56612697-56612747	GM12891	blood:	n/a
12	chr19:56612697-56612747	SK-N-SH_RA	brain:	n/a
13	chr19:56612697-56612747	AG04450	lung:	fetal
14	chr19:56612697-56612747	MCF-7	breast:	n/a
15	chr19:56612697-56612747	U87	brain:	n/a
16	chr19:56612697-56612747	ECC-1	luminal epithelium:	n/a
17	chr19:56612697-56612747	AG09319	gingival:	n/a
18	chr19:56612697-56612747	HNPCEpiC	eye:	n/a
19	chr19:56612697-56612747	HAEpiC	amniotic membrane:	n/a
20	chr19:56612697-56612747	IMR90	lung:	fetal
21	chr19:56612697-56612747	MCF10A-Er-Src	breast:	n/a
22	chr19:56612697-56612747	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:56612697-56612747	SK-N-MC	brain:	n/a
24	chr19:56612697-56612747	AG04449	skin:	fetal
25	chr19:56612697-56612747	Hela-S3	cervix:	n/a
26	chr19:56612697-56612747	SK-N-SH	brain:	n/a
27	chr19:56612697-56612747	A549	lung:	n/a
28	chr19:56612697-56612747	HRPEpiC	eye:	n/a
29	chr19:56612697-56612747	AoSMC	blood vessel:	n/a
30	chr19:56612697-56612747	ovcar-3	ovarian:	n/a
31	chr19:56612697-56612747	GM12878	blood:	n/a
32	chr19:56612697-56612747	BJ	skin:	n/a
33	chr19:56612697-56612747	ProgFib	skin:	n/a
34	chr19:56612697-56612747	H1-hESC	embryonic stem cell:	embryo
35	chr19:56612697-56612747	LNCaP	prostate:	n/a
36	chr19:56612697-56612747	HCM	heart:	n/a
37	chr19:56612697-56612747	PrEC	prostate:	n/a
38	chr19:56612697-56612747	HepG2	liver:	n/a
39	chr19:56612697-56612747	HL-60	blood:	n/a
40	chr19:56612697-56612747	HMEC	breast:	n/a
41	chr19:56612697-56612747	HCT-116	colon:	n/a
42	chr19:56612697-56612747	PFSK-1	brain:	n/a
43	chr19:56612697-56612747	GM06990	blood:	n/a
44	chr19:56612697-56612747	SAEC	small airway:	n/a
45	chr19:56612697-56612747	GM19239	blood:	n/a
46	chr19:56612697-56612747	BE2_C	brain:	n/a
47	chr19:56612697-56612747	HCPEpiC	choroid plexus:	n/a
48	chr19:56612697-56612747	AG10803	skin:	n/a
49	chr19:56612697-56612747	HEK293	kidney:	embryo
50	chr19:56612697-56612747	Jurkat	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56596947..56599631-chr19:56611713..56614011,2	K562	blood:
2	chr19:56609509..56612797-chr19:56648982..56652625,3	K562	blood:
3	chr19:56611899..56614833-chr19:56653450..56656107,2	MCF-7	breast:
4	chr19:56612388..56614679-chr19:57790987..57792726,2	K562	blood:
5	chr19:56612599..56616950-chr19:56825214..56827593,3	MCF-7	breast:
6	chr19:56609156..56614023-chr19:56614843..56617057,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000223060	TF binding region
ENSG00000223060	CpG island
ENSG00000267549	Chromatin interaction
ENSG00000197714	Chromatin interaction
ENSG00000223060	Chromatin interaction
ENSG00000267871	Chromatin interaction
ENSG00000142409	Chromatin interaction
ENSG00000131848	Chromatin interaction
ENSG00000167685	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1007851	0.85[ASN][1000 genomes]
rs12459102	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2450439	0.81[ASN][1000 genomes]
rs2631627	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2631628	0.81[ASN][1000 genomes]
rs2631631	0.83[ASN][1000 genomes]
rs2631637	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2631640	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2637092	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2637094	0.82[ASN][1000 genomes]
rs2637097	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2932757	0.82[ASN][1000 genomes]
rs35766803	0.85[ASN][1000 genomes]
rs473953	0.87[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs478402	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs481936	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs490345	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs492078	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs501798	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs504350	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs506547	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs506782	0.94[EUR][1000 genomes]
rs509897	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs517021	0.81[AMR][1000 genomes]
rs517582	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs521092	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs522980	0.81[AMR][1000 genomes]
rs524778	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs524829	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs524988	0.82[ASN][1000 genomes]
rs525827	0.83[ASN][1000 genomes]
rs526275	0.87[EUR][1000 genomes]
rs527715	0.83[ASN][1000 genomes]
rs530102	1.00[EUR][1000 genomes]
rs533640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs535393	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs536342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs536414	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs537425	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs540900	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs554681	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs564050	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs570210	0.93[ASN][1000 genomes]
rs572851	0.84[ASN][1000 genomes]
rs578990	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs578991	0.89[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs582271	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs583330	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs588574	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs592827	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs604364	0.85[ASN][1000 genomes]
rs609736	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs609755	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs619934	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs626821	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs629544	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs630704	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs640654	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs642776	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs643133	0.83[ASN][1000 genomes]
rs643174	0.81[ASN][1000 genomes]
rs648352	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6509982	0.85[ASN][1000 genomes]
rs659424	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs662308	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs662763	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs665082	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs665846	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs665857	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs667438	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs667974	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs668056	1.00[EUR][1000 genomes]
rs677127	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs677142	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs678540	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs684653	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs685117	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7250351	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056598	chr19:56331762-56703428	Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv580354	chr19:56505685-56723492	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
5	nsv833883	chr19:56512601-56640089	Strong transcription Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv523651	chr19:56537528-56707048	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1057820	chr19:56555942-56720262	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
8	nsv528998	chr19:56578238-56707048	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
9	nsv912512	chr19:56592286-56636759	Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
10	nsv517365	chr19:56592286-56674548	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv912513	chr19:56592286-56685463	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
12	nsv521744	chr19:56592286-56686953	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
13	nsv912514	chr19:56596815-56636759	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
14	nsv912515	chr19:56598829-56623710	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
15	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
16	esv1809307	chr19:56604027-56633623	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	esv1811581	chr19:56609313-56631618	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
18	esv1824038	chr19:56610449-56636632	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56592600-56620000	Weak transcription	HSMMtube	muscle
2	chr19:56592800-56622600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr19:56593000-56616200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr19:56593000-56616600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr19:56593000-56616800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr19:56593000-56631200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr19:56593600-56616000	Weak transcription	Stomach Mucosa	stomach
8	chr19:56594800-56616800	Weak transcription	HUVEC	blood vessel
9	chr19:56596600-56614800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr19:56597200-56619400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr19:56599800-56615200	Strong transcription	Liver	Liver
12	chr19:56600000-56619000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr19:56600400-56614400	Strong transcription	HepG2	liver
14	chr19:56600800-56616800	Weak transcription	Small Intestine	intestine
15	chr19:56602800-56614400	ZNF genes & repeats	Fetal Stomach	stomach
16	chr19:56602800-56620000	Weak transcription	NH-A	brain
17	chr19:56603000-56616600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr19:56603200-56619800	Weak transcription	NHDF-Ad	bronchial
19	chr19:56603800-56616800	Weak transcription	Psoas Muscle	Psoas
20	chr19:56604000-56614800	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr19:56604800-56616200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:56604800-56616800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr19:56605000-56614400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr19:56605000-56615000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:56605000-56616400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:56605200-56615000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr19:56605200-56615000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr19:56605200-56617000	Weak transcription	Brain Angular Gyrus	brain
29	chr19:56605200-56619800	Weak transcription	HSMM	muscle
30	chr19:56605200-56620000	Weak transcription	Fetal Kidney	kidney
31	chr19:56605400-56615000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr19:56605600-56615000	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr19:56605600-56615000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr19:56606000-56615800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr19:56606200-56614200	Strong transcription	Rectal Mucosa Donor 31	rectum
36	chr19:56606200-56615000	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr19:56606200-56615200	Strong transcription	Colonic Mucosa	Colon
38	chr19:56606200-56615200	Strong transcription	Thymus	Thymus
39	chr19:56606400-56613000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr19:56606400-56615200	Strong transcription	Esophagus	oesophagus
41	chr19:56606400-56615200	Strong transcription	A549	lung
42	chr19:56606400-56616600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:56606600-56614400	Strong transcription	Stomach Smooth Muscle	stomach
44	chr19:56606800-56614000	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr19:56606800-56614000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr19:56606800-56614200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr19:56606800-56614600	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr19:56607000-56613000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr19:56607000-56614600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr19:56607000-56615000	Strong transcription	Primary T helper cells fromperipheralblood	blood

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