Variant report

Variant	nsv9722
Chromosome Location	chr19:39298073-39307573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:90)
CpG islands
(count:489)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:90 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr19:39298138-39298148	K562	blood:	n/a	n/a
2	CHD2	chr19:39306333-39306533	H1-hESC	embryonic stem cell:	n/a	n/a
3	CREB1	chr19:39300418-39300724	A549	lung:	n/a	n/a
4	CTCF	chr19:39298490-39298514	Lung_OC	lung:	n/a	n/a
5	CTCF	chr19:39299070-39299146	LNCaP	prostate:	n/a	n/a
6	CTCF	chr19:39298136-39298222	Spleen_OC	spleen:	n/a	n/a
7	CTCF	chr19:39303645-39303836	Pancreas_OC	pancreas:	n/a	n/a
8	E2F6	chr19:39299224-39299718	H1-hESC	embryonic stem cell:	n/a	chr19:39299629-39299639
9	FOS	chr19:39307551-39307600	MCF10A-Er-Src	breast:	n/a	chr19:39307551-39307559
10	FOXA2	chr19:39298227-39298738	A549	lung:	n/a	n/a
11	FOXA2	chr19:39298236-39298782	A549	lung:	n/a	n/a
12	GATA2	chr19:39298286-39298625	K562	blood:	n/a	n/a
13	HMGN3	chr19:39306958-39307048	K562	blood:	n/a	n/a
14	HMGN3	chr19:39305910-39305917	K562	blood:	n/a	n/a
15	JUND	chr19:39307564-39307842	HepG2	liver:	n/a	chr19:39307694-39307705 chr19:39307695-39307704 chr19:39307696-39307703
16	MAX	chr19:39298362-39298599	K562	blood:	n/a	n/a
17	MAX	chr19:39306156-39306575	H1-hESC	embryonic stem cell:	n/a	n/a
18	MAX	chr19:39303990-39304284	K562	blood:	n/a	n/a
19	MAX	chr19:39298430-39298541	K562	blood:	n/a	n/a
20	MYC	chr19:39298472-39298503	K562	blood:	n/a	n/a
21	MYC	chr19:39298513-39298541	K562	blood:	n/a	n/a
22	NFYA	chr19:39306338-39306566	K562	blood:	n/a	chr19:39306468-39306483 chr19:39306401-39306419 chr19:39306401-39306416 chr19:39306433-39306451 chr19:39306401-39306416 chr19:39306468-39306483 chr19:39306469-39306483 chr19:39306401-39306415 chr19:39306464-39306482 chr19:39306400-39306412 chr19:39306470-39306483
23	NFYB	chr19:39306284-39306590	K562	blood:	n/a	chr19:39306468-39306483 chr19:39306401-39306416 chr19:39306401-39306416 chr19:39306468-39306483 chr19:39306469-39306483 chr19:39306401-39306415 chr19:39306400-39306412 chr19:39306470-39306483
24	NFYB	chr19:39306430-39306436	GM12878	blood:	n/a	n/a
25	NR2F2	chr19:39298270-39298820	K562	blood:	n/a	n/a
26	NR2F2	chr19:39298342-39298778	K562	blood:	n/a	n/a
27	NR3C1	chr19:39298414-39298663	A549	lung:	n/a	n/a
28	NR3C1	chr19:39298290-39298697	A549	lung:	n/a	n/a
29	NR3C1	chr19:39298214-39298728	A549	lung:	n/a	n/a
30	NR3C1	chr19:39298214-39298705	A549	lung:	n/a	n/a
31	NR3C1	chr19:39298358-39298697	A549	lung:	n/a	n/a
32	POLR2A	chr19:39305048-39305289	HepG2	liver:	n/a	n/a
33	POLR2A	chr19:39307278-39307684	GM12891	blood:	n/a	n/a
34	POLR2A	chr19:39305521-39306043	GM12892	blood:	n/a	n/a
35	POLR2A	chr19:39307332-39307747	HL-60	blood:	n/a	n/a
36	POLR2A	chr19:39304680-39304979	HepG2	liver:	n/a	n/a
37	POLR2A	chr19:39305621-39306048	GM12892	blood:	n/a	n/a
38	POLR2A	chr19:39305412-39306266	HepG2	liver:	n/a	n/a
39	POLR2A	chr19:39303105-39303252	HepG2	liver:	n/a	n/a
40	POLR2A	chr19:39307401-39307537	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr19:39307144-39307157	HepG2	liver:	n/a	n/a
42	POLR2A	chr19:39307456-39307474	K562	blood:	n/a	n/a
43	POLR2A	chr19:39305712-39306077	K562	blood:	n/a	n/a
44	POLR2A	chr19:39305567-39305884	HepG2	liver:	n/a	n/a
45	POLR2A	chr19:39307537-39307730	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr19:39303445-39303488	K562	blood:	n/a	n/a
47	POLR2A	chr19:39303892-39303974	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr19:39302778-39313143	PANC-1	pancreas:	n/a	n/a
49	POLR2A	chr19:39303996-39304025	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr19:39305590-39306160	HL-60	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39304271-39304321	BE2_C	brain:	n/a
2	chr19:39304271-39304321	BE2_C	brain:	n/a
3	chr19:39306244-39306294	HNPCEpiC	eye:	n/a
4	chr19:39303506-39303556	NT2-D1	testis:	n/a
5	chr19:39303993-39304043	PFSK-1	brain:	n/a
6	chr19:39305100-39305150	AoSMC	blood vessel:	n/a
7	chr19:39303506-39303556	NHDF-neo	bronchial:	n/a
8	chr19:39303993-39304043	HCPEpiC	choroid plexus:	n/a
9	chr19:39303775-39303825	NH-A	brain:	n/a
10	chr19:39303698-39303748	NH-A	brain:	n/a
11	chr19:39306244-39306294	MCF-7	breast:	n/a
12	chr19:39303775-39303825	T-47D	breast:	n/a
13	chr19:39303993-39304043	GM19239	blood:	n/a
14	chr19:39299581-39299631	PFSK-1	brain:	n/a
15	chr19:39305100-39305150	SK-N-SH	brain:	n/a
16	chr19:39303775-39303825	HNPCEpiC	eye:	n/a
17	chr19:39303506-39303556	Jurkat	blood:	n/a
18	chr19:39303698-39303748	SK-N-SH	brain:	n/a
19	chr19:39303506-39303556	SK-N-SH	brain:	n/a
20	chr19:39305100-39305150	HEEpiC	esophagus:	n/a
21	chr19:39303506-39303556	LNCaP	prostate:	n/a
22	chr19:39303506-39303556	HRE	kidney:	n/a
23	chr19:39303698-39303748	HIPEpiC	eye:	n/a
24	chr19:39299581-39299631	HepG2	liver:	n/a
25	chr19:39303775-39303825	H1-hESC	embryonic stem cell:	embryo
26	chr19:39304271-39304321	Caco-2	colon:	n/a
27	chr19:39303993-39304043	NH-A	brain:	n/a
28	chr19:39306244-39306294	ECC-1	luminal epithelium:	n/a
29	chr19:39303775-39303825	MCF10A-Er-Src	breast:	n/a
30	chr19:39303775-39303825	ovcar-3	ovarian:	n/a
31	chr19:39304271-39304321	NHBE	bronchial:	n/a
32	chr19:39303993-39304043	NB4	blood:	n/a
33	chr19:39303993-39304043	A549	lung:	n/a
34	chr19:39299581-39299631	HMEC	breast:	n/a
35	chr19:39303775-39303825	BE2_C	brain:	n/a
36	chr19:39303993-39304043	MCF10A-Er-Src	breast:	n/a
37	chr19:39303993-39304043	MCF-7	breast:	n/a
38	chr19:39305100-39305150	T-47D	breast:	n/a
39	chr19:39299581-39299631	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:39305100-39305150	HCPEpiC	choroid plexus:	n/a
41	chr19:39303698-39303748	Hela-S3	cervix:	n/a
42	chr19:39304271-39304321	PrEC	prostate:	n/a
43	chr19:39305100-39305150	BJ	skin:	n/a
44	chr19:39303993-39304043	HCM	heart:	n/a
45	chr19:39306244-39306294	K562	blood:	n/a
46	chr19:39306244-39306294	U87	brain:	n/a
47	chr19:39306244-39306294	AG09319	gingival:	n/a
48	chr19:39304271-39304321	NT2-D1	testis:	n/a
49	chr19:39306244-39306294	MCF10A-Er-Src	breast:	n/a
50	chr19:39306244-39306294	HRPEpiC	eye:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39305126..39308258-chr19:39321941..39324366,4	K562	blood:
2	chr19:39278557..39281313-chr19:39305805..39307829,2	MCF-7	breast:
3	chr19:39306612..39310061-chr19:39334754..39339038,4	K562	blood:
4	chr19:39305724..39308620-chr19:39308879..39311363,2	K562	blood:
5	chr19:39303539..39306224-chr19:39328570..39331543,2	MCF-7	breast:
6	chr19:39305724..39308270-chr19:39309702..39311363,2	K562	blood:
7	chr19:39304217..39307847-chr19:39338556..39341715,3	MCF-7	breast:
8	chr19:39295644..39297355-chr19:39298122..39300967,2	MCF-7	breast:
9	chr19:39306785..39309520-chr19:39336164..39339038,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268756	TF binding region
LGALS4	TF binding region
ECH1	TF binding region
ENSG00000268756	CpG island
LGALS4	CpG island
ECH1	CpG island
ENSG00000104824	chromatin interactions
ENSG00000269688	chromatin interactions
ENSG00000268756	chromatin interactions
ENSG00000171747	chromatin interactions
ENSG00000104823	chromatin interactions
ENSG00000178934	chromatin interactions

Extended variants
information (count: 458 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12972114	chr19:39298137-39298138	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148101155	chr19:39298153-39298154	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs527719656	chr19:39298154-39298155	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141746158	chr19:39298158-39298159	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs59965320	chr19:39298192-39298193	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs550752369	chr19:39298196-39298197	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568970683	chr19:39298197-39298198	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs533014526	chr19:39298201-39298202	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551224753	chr19:39298202-39298203	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546075268	chr19:39298210-39298211	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566457106	chr19:39298223-39298224	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs552893004	chr19:39298233-39298234	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533592104	chr19:39298275-39298276	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187381938	chr19:39298283-39298284	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564842360	chr19:39298285-39298286	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572951792	chr19:39298301-39298302	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538165587	chr19:39298316-39298317	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs565838540	chr19:39298365-39298366	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs556311711	chr19:39298376-39298377	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543664604	chr19:39298381-39298382	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs578131316	chr19:39298397-39298398	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs192106321	chr19:39298399-39298400	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10417292	chr19:39298414-39298415	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs572399817	chr19:39298422-39298423	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542996513	chr19:39298460-39298461	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561273295	chr19:39298461-39298462	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529165662	chr19:39298468-39298469	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs529410549	chr19:39298517-39298518	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs112855651	chr19:39298521-39298522	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs111562024	chr19:39298527-39298528	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533021964	chr19:39298548-39298549	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs183469198	chr19:39298551-39298552	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186845762	chr19:39298571-39298572	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs527395289	chr19:39298621-39298622	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs113718174	chr19:39298636-39298637	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538128073	chr19:39298702-39298703	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs576091878	chr19:39298782-39298783	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190097889	chr19:39298791-39298792	Weak transcription Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536212041	chr19:39298819-39298820	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs144947382	chr19:39298914-39298915	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554346189	chr19:39298972-39298973	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs572529106	chr19:39298987-39298988	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12463099	chr19:39298989-39298990	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs182607537	chr19:39298999-39299000	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576530746	chr19:39299002-39299003	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148629764	chr19:39299038-39299039	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551874911	chr19:39299054-39299055	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs142942401	chr19:39299056-39299057	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187279917	chr19:39299066-39299067	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs544838679	chr19:39299124-39299125	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:343 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39283200-39305600	Weak transcription	Brain Angular Gyrus	brain
2	chr19:39283200-39305600	Weak transcription	Brain Substantia Nigra	brain
3	chr19:39283600-39305600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr19:39283600-39305800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr19:39283600-39305800	Weak transcription	Brain Hippocampus Middle	brain
6	chr19:39283600-39305800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr19:39283800-39306000	Weak transcription	Primary B cells from cord blood	blood
8	chr19:39284000-39305600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:39284000-39318200	Weak transcription	Fetal Kidney	kidney
10	chr19:39284200-39305800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr19:39285200-39309400	Weak transcription	Fetal Heart	heart
12	chr19:39290200-39305800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr19:39290800-39310600	Weak transcription	HMEC	breast
14	chr19:39291200-39307400	Weak transcription	Fetal Lung	lung
15	chr19:39291400-39305600	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr19:39292000-39305800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr19:39292400-39300400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr19:39292600-39301800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr19:39292600-39303800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr19:39292600-39305800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr19:39292800-39303800	Weak transcription	Fetal Muscle Leg	muscle
22	chr19:39292800-39305800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:39292800-39306000	Weak transcription	Brain Anterior Caudate	brain
24	chr19:39293000-39305200	Weak transcription	Primary T cells from cord blood	blood
25	chr19:39294400-39299400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:39294400-39301800	Weak transcription	Small Intestine	intestine
27	chr19:39294600-39309800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr19:39294800-39299400	Weak transcription	Gastric	stomach
29	chr19:39294800-39302600	Weak transcription	Liver	Liver
30	chr19:39294800-39309800	Weak transcription	Psoas Muscle	Psoas
31	chr19:39295000-39300400	Weak transcription	Pancreas	Pancrea
32	chr19:39295000-39303000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr19:39295000-39303000	Weak transcription	Placenta	Placenta
34	chr19:39295000-39305600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr19:39295000-39305800	Weak transcription	Adipose Nuclei	Adipose
36	chr19:39295200-39302800	Weak transcription	Fetal Stomach	stomach
37	chr19:39296000-39300400	Genic enhancers	Fetal Intestine Small	intestine
38	chr19:39296000-39305800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr19:39296200-39305000	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr19:39296200-39307000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr19:39296200-39318200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr19:39296400-39298200	Genic enhancers	Duodenum Mucosa	Duodenum
43	chr19:39296400-39298800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr19:39296400-39299000	Weak transcription	Lung	lung
45	chr19:39296400-39299200	Weak transcription	Spleen	Spleen
46	chr19:39296400-39299400	Weak transcription	Colonic Mucosa	Colon
47	chr19:39296400-39301000	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr19:39296400-39304200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr19:39296400-39305600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr19:39296400-39305600	Weak transcription	Ovary	ovary

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