Variant report

Variant	esv3329584
Chromosome Location	chr19:39196712-39204110
allele	n/a
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	BCL3	chr19:39202304-39203550	A549	lung:	n/a	chr19:39202565-39202573
2	BCL3	chr19:39203847-39204851	A549	lung:	n/a	n/a
3	BCL3	chr19:39200946-39202180	A549	lung:	n/a	n/a
4	BCL3	chr19:39196079-39197246	A549	lung:	n/a	n/a
5	CEBPB	chr19:39201899-39202702	IMR90	lung:	n/a	n/a
6	CTCF	chr19:39202400-39202550	HMEC	breast:	n/a	chr19:39202485-39202498
7	CTCF	chr19:39198280-39198430	HUVEC	blood vessel:	n/a	n/a
8	CTCF	chr19:39202440-39202590	AG04450	lung:	n/a	chr19:39202485-39202498
9	CTCF	chr19:39202420-39202570	HPF	lung:	n/a	chr19:39202485-39202498
10	CTCF	chr19:39202436-39202577	Fibrobl	skin:	n/a	chr19:39202485-39202498
11	CTCF	chr19:39202400-39202550	HCPEpiC	choroid plexus:	n/a	chr19:39202485-39202498
12	CTCF	chr19:39202380-39202530	WI-38	lung:	n/a	chr19:39202485-39202498
13	CTCF	chr19:39202440-39202567	ProgFib	skin:	n/a	chr19:39202485-39202498
14	CTCF	chr19:39202220-39202470	HFF	foreskin:	n/a	n/a
15	CTCF	chr19:39202360-39202510	NHDF-neo	bronchial:	n/a	chr19:39202485-39202498
16	CTCF	chr19:39202475-39202537	NHEK	skin:	n/a	chr19:39202485-39202498
17	CTCF	chr19:39202400-39202550	HMF	breast:	n/a	chr19:39202485-39202498
18	CTCF	chr19:39202500-39202650	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr19:39202420-39202570	HBMEC	blood vessel:	n/a	chr19:39202485-39202498
20	CTCF	chr19:39202420-39202570	AG04449	skin:	n/a	chr19:39202485-39202498
21	CTCF	chr19:39202220-39202370	HAc	cerebellar:	n/a	n/a
22	CTCF	chr19:39202460-39202610	HCFaa	heart:	n/a	chr19:39202485-39202498
23	CTCF	chr19:39202380-39202530	HPAF	blood vessel:	n/a	chr19:39202485-39202498
24	CTCF	chr19:39202981-39203007	GM12891	blood:	n/a	n/a
25	CTCF	chr19:39202400-39202550	HA-sp	spinal cord:	n/a	chr19:39202485-39202498
26	CTCF	chr19:39202400-39202550	AG10803	skin:	n/a	chr19:39202485-39202498
27	CTCF	chr19:39202400-39202550	HVMF	connective:	n/a	chr19:39202485-39202498
28	CTCF	chr19:39198365-39198461	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr19:39202560-39202710	GM12865	blood:	n/a	n/a
30	CTCF	chr19:39202400-39202550	SAEC	small airway:	n/a	chr19:39202485-39202498
31	CTCF	chr19:39202400-39202550	HRPEpiC	eye:	n/a	chr19:39202485-39202498
32	CTCF	chr19:39202420-39202570	AG09319	gingival:	n/a	chr19:39202485-39202498
33	CTCF	chr19:39202440-39202590	HBMEC	blood vessel:	n/a	chr19:39202485-39202498
34	CTCF	chr19:39202953-39203031	GM12892	blood:	n/a	n/a
35	CTCF	chr19:39202400-39202550	HPF	lung:	n/a	chr19:39202485-39202498
36	CTCF	chr19:39202440-39202590	AG09309	skin:	n/a	chr19:39202485-39202498
37	CTCF	chr19:39198180-39198330	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr19:39202338-39202674	IMR90	lung:	n/a	chr19:39202485-39202498
39	CTCF	chr19:39202440-39202590	AG04449	skin:	n/a	chr19:39202485-39202498
40	CTCF	chr19:39202520-39202670	AG04450	lung:	n/a	n/a
41	CTCF	chr19:39202420-39202570	HMF	breast:	n/a	chr19:39202485-39202498
42	CTCF	chr19:39202500-39202650	BJ	skin:	n/a	n/a
43	CTCF	chr19:39202460-39202610	HCPEpiC	choroid plexus:	n/a	chr19:39202485-39202498
44	CTCF	chr19:39202240-39202390	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr19:39202600-39202750	WI-38	lung:	n/a	n/a
46	CTCF	chr19:39202480-39202630	HAc	cerebellar:	n/a	chr19:39202485-39202498
47	CTCF	chr19:39202480-39202630	BJ	skin:	n/a	chr19:39202485-39202498
48	CTCF	chr19:39202440-39202590	HMEC	breast:	n/a	chr19:39202485-39202498
49	CTCF	chr19:39202461-39202542	Gliobla	brain:	n/a	chr19:39202485-39202498
50	CTCF	chr19:39202420-39202570	RPTEC	kidney:	n/a	chr19:39202485-39202498

No.	Distal block	Cell Line	Cell type
1	chr19:39189791..39192031-chr19:39202045..39204236,3	MCF-7	breast:
2	chr19:39136969..39142530-chr19:39203025..39206877,12	MCF-7	breast:
3	chr19:39188988..39191568-chr19:39196773..39198284,2	K562	blood:
4	chr19:39193152..39194811-chr19:39195502..39197408,2	MCF-7	breast:
5	chr19:39170809..39173774-chr19:39199187..39201318,2	K562	blood:
6	chr19:39173657..39176403-chr19:39201609..39205956,8	MCF-7	breast:
7	chr19:39151900..39153408-chr19:39203433..39205156,2	MCF-7	breast:
8	chr19:39156320..39158010-chr19:39194511..39197034,2	MCF-7	breast:
9	chr19:39138096..39140426-chr19:39194942..39197534,2	K562	blood:
10	chr19:39203079..39204604-chr19:39326634..39328789,2	MCF-7	breast:
11	chr19:39177569..39179808-chr19:39201559..39205279,5	MCF-7	breast:
12	chr19:39195090..39197798-chr19:39197954..39200910,2	K562	blood:
13	chr19:39196541..39198571-chr19:39208360..39211296,2	K562	blood:
14	chr19:39198080..39199648-chr19:39203544..39206243,2	K562	blood:
15	chr19:39198023..39200060-chr19:39200428..39202731,2	K562	blood:
16	chr19:39198023..39200060-chr19:39200428..39202731,2	K562	blood:
17	chr19:39125626..39127336-chr19:39202058..39204269,2	K562	blood:
18	chr19:39202818..39205555-chr19:39206868..39209450,2	K562	blood:
19	chr19:39200022..39202960-chr19:39340126..39342618,2	K562	blood:
20	chr19:39125533..39130601-chr19:39201644..39207054,6	MCF-7	breast:
21	chr19:39201322..39204125-chr19:39215978..39220088,5	K562	blood:
22	chr19:39135966..39142009-chr19:39184894..39201240,23	MCF-7	breast:
23	chr19:39154055..39157137-chr19:39203619..39206563,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS7B-3	chr19:39201473-39202001	NONHSAT066231
2	lnc-LGALS7B-2	chr19:39203997-39204367	NONHSAT066232

Variant related genes	Relation type
ACTN4	TF binding region
ENSG00000104824	chromatin interactions
ENSG00000130402	chromatin interactions

Extended variants
information (count: 318 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149027682	chr19:39196735-39196736	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs11553600	chr19:39196736-39196737	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs3745859	chr19:39196745-39196746	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs571812757	chr19:39196746-39196747	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs202126611	chr19:39196750-39196751	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs145730643	chr19:39196776-39196777	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs60710743	chr19:39196782-39196783	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs200442845	chr19:39196794-39196795	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs555388589	chr19:39196821-39196822	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs567413755	chr19:39196858-39196859	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537646804	chr19:39196903-39196904	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs556220518	chr19:39196920-39196921	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577359710	chr19:39196921-39196922	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs138744742	chr19:39196938-39196939	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs553380979	chr19:39196985-39196986	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs571733186	chr19:39196986-39196987	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374345491	chr19:39197017-39197018	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs112614234	chr19:39197018-39197019	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs183599374	chr19:39197057-39197058	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188361522	chr19:39197080-39197081	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs35729716	chr19:39197102-39197103	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs12459757	chr19:39197172-39197173	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs543692435	chr19:39197193-39197194	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371201099	chr19:39197235-39197236	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs8104815	chr19:39197310-39197311	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs367893114	chr19:39197345-39197346	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs74995758	chr19:39197386-39197387	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs8105055	chr19:39197502-39197503	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs566044261	chr19:39197513-39197514	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs8105069	chr19:39197527-39197528	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs549213060	chr19:39197530-39197531	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs8105080	chr19:39197552-39197553	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs181809445	chr19:39197584-39197585	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs6508814	chr19:39197585-39197586	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs570990140	chr19:39197640-39197641	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs11882006	chr19:39197643-39197644	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs142726826	chr19:39197722-39197723	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs8105216	chr19:39197729-39197730	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs8105550	chr19:39197773-39197774	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs549329775	chr19:39197808-39197809	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542263985	chr19:39197847-39197848	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147301485	chr19:39197895-39197896	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576696202	chr19:39197925-39197926	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs35856174	chr19:39197954-39197955	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs543681882	chr19:39197983-39197984	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs61432695	chr19:39197984-39197985	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs139231631	chr19:39198060-39198061	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141599452	chr19:39198152-39198153	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs150898429	chr19:39198153-39198154	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546819236	chr19:39198215-39198216	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	19151661	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39164400-39200200	Genic enhancers	Fetal Intestine Small	intestine
2	chr19:39178600-39198200	Genic enhancers	Fetal Intestine Large	intestine
3	chr19:39179600-39205800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr19:39182200-39214200	Genic enhancers	Fetal Muscle Trunk	muscle
5	chr19:39182200-39225200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr19:39184800-39205800	Genic enhancers	A549	lung
7	chr19:39185200-39205800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr19:39186400-39213400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr19:39187200-39201200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
10	chr19:39187200-39205800	Genic enhancers	Right Ventricle	heart
11	chr19:39187800-39198600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr19:39189400-39223400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr19:39189800-39198200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr19:39189800-39222800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:39190000-39203800	Strong transcription	H9 Cell Line	embryonic stem cell
16	chr19:39190000-39205800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr19:39190000-39208800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr19:39190000-39218400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr19:39190200-39222600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr19:39190200-39222800	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr19:39190400-39206000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr19:39190400-39208400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr19:39190400-39209200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr19:39190400-39212000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr19:39190400-39212200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:39190400-39217000	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr19:39190400-39218000	Strong transcription	Primary T cells from cord blood	blood
28	chr19:39190400-39222400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr19:39190400-39222600	Strong transcription	Dnd41	blood
30	chr19:39190600-39199800	Strong transcription	NHEK	skin
31	chr19:39190600-39202800	Strong transcription	GM12878-XiMat	blood
32	chr19:39190600-39203200	Strong transcription	K562	blood
33	chr19:39190600-39205400	Genic enhancers	Spleen	Spleen
34	chr19:39190600-39205600	Strong transcription	Fetal Brain Female	brain
35	chr19:39190600-39209000	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr19:39190600-39209200	Strong transcription	Placenta Amnion	Placenta Amnion
37	chr19:39190600-39216400	Strong transcription	Primary T cells fromperipheralblood	blood
38	chr19:39190600-39217000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr19:39190600-39219600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr19:39190600-39222800	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr19:39190800-39220400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr19:39190800-39222600	Strong transcription	Primary B cells from peripheral blood	blood
43	chr19:39190800-39222600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:39190800-39222800	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr19:39190800-39223000	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr19:39190800-39223000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:39191000-39203200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr19:39191000-39205800	Genic enhancers	Left Ventricle	heart
49	chr19:39191000-39222400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr19:39191000-39222600	Strong transcription	Monocytes-CD14+_RO01746	blood

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