Variant report

Variant	nsv961215
Chromosome Location	chr19:39329561-39331790
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	chr19:39327233-39330842	A549	lung:	n/a	chr19:39328370-39328379
2	BCL3	chr19:39329044-39330454	A549	lung:	n/a	n/a
3	BRCA1	chr19:39331416-39331462	HepG2	liver:	n/a	n/a
4	CTCF	chr19:39329440-39329590	HMEC	breast:	n/a	n/a
5	CTCF	chr19:39329455-39329584	MCF-7	breast:	n/a	n/a
6	CTCF	chr19:39329440-39329590	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr19:39329460-39329610	HCT-116	colon:	n/a	n/a
8	CTCF	chr19:39329440-39329590	MCF-7	breast:	n/a	n/a
9	CTCF	chr19:39329434-39329606	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr19:39329420-39329570	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr19:39329460-39329610	Caco-2	colon:	n/a	n/a
12	CTCF	chr19:39329480-39329630	NHEK	skin:	n/a	n/a
13	CTCF	chr19:39329420-39329570	HMEC	breast:	n/a	n/a
14	CTCF	chr19:39329480-39329630	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr19:39329440-39329590	HRE	kidney:	n/a	n/a
16	CTCF	chr19:39329560-39329710	A549	lung:	n/a	n/a
17	CTCF	chr19:39329460-39329610	NHEK	skin:	n/a	n/a
18	CTCF	chr19:39329480-39329630	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr19:39329441-39329584	MCF-7	breast:	n/a	n/a
20	CTCF	chr19:39329480-39329630	HAc	cerebellar:	n/a	n/a
21	CTCF	chr19:39329400-39329624	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:39329440-39329590	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr19:39329440-39329594	MCF-7	breast:	n/a	n/a
24	CTCF	chr19:39329446-39329588	MCF-7	breast:	n/a	n/a
25	CTCF	chr19:39329306-39329670	NHEK	skin:	n/a	n/a
26	ELF1	chr19:39329155-39329804	A549	lung:	n/a	n/a
27	EP300	chr19:39328109-39329650	A549	lung:	n/a	chr19:39328438-39328445 chr19:39328370-39328379
28	FOS	chr19:39329200-39329619	MCF10A-Er-Src	breast:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
29	FOS	chr19:39330537-39330740	MCF10A-Er-Src	breast:	n/a	chr19:39330612-39330622 chr19:39330612-39330622 chr19:39330613-39330621 chr19:39330612-39330622 chr19:39330612-39330622
30	FOS	chr19:39329182-39329603	MCF10A-Er-Src	breast:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
31	FOS	chr19:39330480-39330680	MCF10A-Er-Src	breast:	n/a	chr19:39330612-39330622 chr19:39330612-39330622 chr19:39330613-39330621 chr19:39330612-39330622 chr19:39330612-39330622
32	FOS	chr19:39330529-39330780	MCF10A-Er-Src	breast:	n/a	chr19:39330612-39330622 chr19:39330612-39330622 chr19:39330613-39330621 chr19:39330612-39330622 chr19:39330612-39330622
33	FOS	chr19:39329181-39329610	MCF10A-Er-Src	breast:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
34	FOS	chr19:39329192-39329630	MCF10A-Er-Src	breast:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
35	FOS	chr19:39330425-39330767	MCF10A-Er-Src	breast:	n/a	chr19:39330612-39330622 chr19:39330612-39330622 chr19:39330613-39330621 chr19:39330612-39330622 chr19:39330612-39330622
36	FOSL1	chr19:39329181-39329753	HCT-116	colon:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
37	FOSL2	chr19:39329149-39329708	MCF-7	breast:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
38	FOSL2	chr19:39329163-39329613	HepG2	liver:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
39	FOSL2	chr19:39329192-39329691	MCF-7	breast:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
40	FOSL2	chr19:39329157-39329745	A549	lung:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
41	FOSL2	chr19:39329064-39329982	A549	lung:	n/a	chr19:39329364-39329374 chr19:39329425-39329437 chr19:39329365-39329373 chr19:39329364-39329374 chr19:39329363-39329375
42	GATA3	chr19:39329202-39329726	MCF-7	breast:	n/a	chr19:39329430-39329439
43	GATA3	chr19:39327959-39329768	MCF-7	breast:	n/a	chr19:39329430-39329439
44	GATA3	chr19:39327931-39329823	A549	lung:	n/a	chr19:39329430-39329439
45	HEY1	chr19:39329521-39329935	HepG2	liver:	n/a	n/a
46	HEY1	chr19:39328842-39330408	K562	blood:	n/a	n/a
47	HEY1	chr19:39330486-39330823	K562	blood:	n/a	n/a
48	HEY1	chr19:39331327-39331597	HepG2	liver:	n/a	n/a
49	HEY1	chr19:39330078-39330416	HepG2	liver:	n/a	n/a
50	HEY1	chr19:39331676-39331888	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:39216544..39219007-chr19:39328306..39331285,2	MCF-7	breast:
2	chr19:39137231..39139589-chr19:39329369..39331157,2	MCF-7	breast:
3	chr19:39303539..39306224-chr19:39328570..39331543,2	MCF-7	breast:
4	chr19:39181974..39184740-chr19:39331353..39332941,2	MCF-7	breast:
5	chr19:39217938..39222423-chr19:39330106..39333750,7	K562	blood:
6	chr19:39137584..39140325-chr19:39327324..39331607,4	MCF-7	breast:
7	chr19:39223964..39228282-chr19:39327392..39332302,8	MCF-7	breast:
8	chr19:39328430..39329992-chr19:39354096..39356995,2	MCF-7	breast:
9	chr19:39218553..39228703-chr19:39324875..39331730,17	MCF-7	breast:
10	chr19:39326367..39329872-chr19:39419342..39422625,3	MCF-7	breast:

Variant related genes	Relation type
HNRNPL	TF binding region
ENSG00000268083	TF binding region
ENSG00000267375	chromatin interactions
ENSG00000130402	chromatin interactions
ENSG00000182472	chromatin interactions
ENSG00000171747	chromatin interactions
ENSG00000128626	chromatin interactions
ENSG00000104835	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370003343	chr19:39329579-39329580	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs200815731	chr19:39329584-39329585	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs142725492	chr19:39329599-39329600	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs148046358	chr19:39329626-39329627	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs372302259	chr19:39329632-39329633	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs535615136	chr19:39329661-39329662	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs113878198	chr19:39329668-39329669	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs375728875	chr19:39329688-39329689	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs75450845	chr19:39329717-39329718	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs550948499	chr19:39329730-39329731	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs544280273	chr19:39329773-39329774	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs539852555	chr19:39329774-39329775	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs111990928	chr19:39329858-39329859	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs577232775	chr19:39329882-39329883	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs138853456	chr19:39329894-39329895	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs550065375	chr19:39329901-39329902	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs552929532	chr19:39329928-39329929	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs141268532	chr19:39329936-39329937	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs541511779	chr19:39329958-39329959	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs75120679	chr19:39329963-39329964	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs574856170	chr19:39329970-39329971	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs370185009	chr19:39329971-39329972	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs150767687	chr19:39329980-39329981	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs139215397	chr19:39329998-39329999	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs561754568	chr19:39330013-39330014	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs528793170	chr19:39330044-39330045	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs374130822	chr19:39330047-39330048	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs10403012	chr19:39330058-39330059	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs547608420	chr19:39330065-39330066	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs562189969	chr19:39330088-39330089	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs146657722	chr19:39330136-39330137	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs149536118	chr19:39330175-39330176	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs569389383	chr19:39330267-39330268	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs183833266	chr19:39330296-39330297	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs373939601	chr19:39330297-39330298	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs551830671	chr19:39330348-39330349	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs73930210	chr19:39330352-39330353	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs114543737	chr19:39330386-39330387	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs73930211	chr19:39330391-39330392	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs568120038	chr19:39330402-39330403	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs192591702	chr19:39330403-39330404	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs571321507	chr19:39330420-39330421	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs556751081	chr19:39330433-39330434	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs147151117	chr19:39330513-39330514	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs545377952	chr19:39330536-39330537	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs557371329	chr19:39330552-39330553	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs573196332	chr19:39330558-39330559	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs377264472	chr19:39330572-39330573	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs372338866	chr19:39330625-39330626	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs562415807	chr19:39330626-39330627	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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

Chromatin state (count:186 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39322400-39331800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:39323000-39334600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr19:39324600-39338000	Strong transcription	Fetal Brain Female	brain
4	chr19:39325000-39334000	Strong transcription	Fetal Stomach	stomach
5	chr19:39325200-39331600	Strong transcription	Primary T cells from cord blood	blood
6	chr19:39325400-39329800	Genic enhancers	Fetal Lung	lung
7	chr19:39325400-39331200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr19:39325400-39331600	Strong transcription	Fetal Thymus	thymus
9	chr19:39325400-39332000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr19:39325400-39332200	Strong transcription	Thymus	Thymus
11	chr19:39325400-39336800	Strong transcription	Brain Substantia Nigra	brain
12	chr19:39325400-39337800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:39325400-39337800	Strong transcription	Brain Cingulate Gyrus	brain
14	chr19:39325400-39338000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr19:39325400-39338200	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr19:39325400-39338200	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr19:39325600-39333600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:39325600-39338000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:39325800-39330800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr19:39326000-39331000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr19:39326000-39331200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr19:39326000-39332200	Genic enhancers	Placenta	Placenta
23	chr19:39326000-39332600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr19:39326000-39332600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr19:39326000-39333800	Strong transcription	Colonic Mucosa	Colon
26	chr19:39326000-39334000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr19:39326000-39336200	Strong transcription	Brain Hippocampus Middle	brain
28	chr19:39326000-39336600	Strong transcription	Duodenum Smooth Muscle	Duodenum
29	chr19:39326000-39337000	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr19:39326000-39337800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr19:39326000-39338000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr19:39326000-39338000	Strong transcription	Brain Anterior Caudate	brain
33	chr19:39326000-39338000	Strong transcription	HSMM	muscle
34	chr19:39326000-39338200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
35	chr19:39326000-39338200	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr19:39326000-39338200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr19:39326000-39338200	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr19:39326000-39338200	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr19:39326000-39338400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
40	chr19:39326000-39338400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr19:39326000-39338600	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr19:39326200-39329600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:39326200-39329800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr19:39326200-39330400	Genic enhancers	Stomach Mucosa	stomach
45	chr19:39326200-39330600	Genic enhancers	Hela-S3	cervix
46	chr19:39326200-39331400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr19:39326200-39331600	Strong transcription	Primary B cells from cord blood	blood
48	chr19:39326200-39331600	Strong transcription	Adipose Nuclei	Adipose
49	chr19:39326200-39331800	Strong transcription	GM12878-XiMat	blood
50	chr19:39326200-39332800	Genic enhancers	HMEC	breast

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