Variant report

Variant	nsv963023
Chromosome Location	chr19:21491992-21570395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1010)
CpG islands
(count:1405)
Chromatin interactive
region (count:18)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21511981-21512446	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21541510-21541771	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:21511352-21511789	K562	blood:	n/a	n/a
4	ARID3A	chr19:21505863-21506155	K562	blood:	n/a	n/a
5	ATF1	chr19:21512075-21512439	K562	blood:	n/a	n/a
6	ATF1	chr19:21516826-21516854	K562	blood:	n/a	n/a
7	ATF2	chr19:21512025-21512405	GM12878	blood:	n/a	n/a
8	BACH1	chr19:21511633-21511637	K562	blood:	n/a	n/a
9	BATF	chr19:21497419-21497765	GM12878	blood:	n/a	chr19:21497586-21497597 chr19:21497587-21497597
10	BATF	chr19:21512047-21512392	GM12878	blood:	n/a	n/a
11	BATF	chr19:21497495-21497696	GM12878	blood:	n/a	chr19:21497586-21497597 chr19:21497587-21497597
12	BCLAF1	chr19:21511741-21512420	GM12878	blood:	n/a	chr19:21511749-21511762
13	BCLAF1	chr19:21511700-21512480	GM12878	blood:	n/a	chr19:21511749-21511762
14	BHLHE40	chr19:21511934-21512494	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:21563870-21563999	K562	blood:	n/a	chr19:21563932-21563945 chr19:21563928-21563949
16	BHLHE40	chr19:21511805-21512401	K562	blood:	n/a	n/a
17	BHLHE40	chr19:21541603-21542196	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:21511144-21511449	GM12878	blood:	n/a	n/a
19	BRCA1	chr19:21511953-21512347	GM12878	blood:	n/a	n/a
20	BRCA1	chr19:21512062-21512389	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr19:21511688-21512473	K562	blood:	n/a	n/a
22	CBX3	chr19:21518494-21518875	K562	blood:	n/a	n/a
23	CBX3	chr19:21512080-21512432	K562	blood:	n/a	n/a
24	CBX3	chr19:21518473-21518918	K562	blood:	n/a	n/a
25	CCNT2	chr19:21511735-21512332	K562	blood:	n/a	n/a
26	CEBPB	chr19:21505077-21505265	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr19:21541467-21541799	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr19:21499024-21499025	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr19:21541453-21541975	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr19:21531522-21531558	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr19:21508950-21509264	IMR90	lung:	n/a	n/a
32	CEBPB	chr19:21541478-21541829	IMR90	lung:	n/a	n/a
33	CEBPB	chr19:21540715-21540842	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr19:21541564-21541741	K562	blood:	n/a	n/a
35	CEBPD	chr19:21511872-21512210	HepG2	liver:	n/a	n/a
36	CEBPD	chr19:21505818-21506226	K562	blood:	n/a	n/a
37	CEBPD	chr19:21505866-21506242	K562	blood:	n/a	n/a
38	CEBPD	chr19:21511987-21512428	K562	blood:	n/a	n/a
39	CHD1	chr19:21511152-21512118	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr19:21541722-21542357	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr19:21511315-21512402	GM12878	blood:	n/a	n/a
42	CHD1	chr19:21541871-21542315	GM12878	blood:	n/a	n/a
43	CHD1	chr19:21542666-21542959	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr19:21511911-21512374	GM12878	blood:	n/a	n/a
45	CHD2	chr19:21511775-21512315	K562	blood:	n/a	n/a
46	CHD2	chr19:21541560-21542185	GM12878	blood:	n/a	n/a
47	CHD2	chr19:21541560-21541985	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr19:21541599-21541809	K562	blood:	n/a	n/a
49	CHD2	chr19:21511821-21512364	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr19:21541566-21542067	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21541537-21541587	AG04449	skin:	fetal
2	chr19:21512191-21512241	HMEC	breast:	n/a
3	chr19:21541537-21541587	AG04449	skin:	fetal
4	chr19:21512191-21512241	HMEC	breast:	n/a
5	chr19:21541765-21541815	SK-N-SH	brain:	n/a
6	chr19:21541035-21541085	HEK293	kidney:	embryo
7	chr19:21541044-21541094	BJ	skin:	n/a
8	chr19:21541756-21541806	HEEpiC	esophagus:	n/a
9	chr19:21512258-21512308	HepG2	liver:	n/a
10	chr19:21540946-21540996	GM12878	blood:	n/a
11	chr19:21513650-21513700	PrEC	prostate:	n/a
12	chr19:21512378-21512428	AG10803	skin:	n/a
13	chr19:21511996-21512046	SK-N-SH_RA	brain:	n/a
14	chr19:21513138-21513188	NB4	blood:	n/a
15	chr19:21541699-21541749	Caco-2	colon:	n/a
16	chr19:21541537-21541587	HIPEpiC	eye:	n/a
17	chr19:21541358-21541408	SK-N-MC	brain:	n/a
18	chr19:21511996-21512046	SK-N-SH	brain:	n/a
19	chr19:21541358-21541408	PFSK-1	brain:	n/a
20	chr19:21541035-21541085	NB4	blood:	n/a
21	chr19:21540946-21540996	HRCEpiC	kidney:	n/a
22	chr19:21541358-21541408	HRCEpiC	kidney:	n/a
23	chr19:21512191-21512241	HAEpiC	amniotic membrane:	n/a
24	chr19:21541699-21541749	NT2-D1	testis:	n/a
25	chr19:21541699-21541749	GM06990	blood:	n/a
26	chr19:21512141-21512191	LNCaP	prostate:	n/a
27	chr19:21540538-21540588	NT2-D1	testis:	n/a
28	chr19:21540946-21540996	GM19239	blood:	n/a
29	chr19:21513138-21513188	K562	blood:	n/a
30	chr19:21541699-21541749	SK-N-SH_RA	brain:	n/a
31	chr19:21541699-21541749	HL-60	blood:	n/a
32	chr19:21513138-21513188	HRPEpiC	eye:	n/a
33	chr19:21512378-21512428	HPAEpiC	pulmonary alveolar:	n/a
34	chr19:21511996-21512046	AG09319	gingival:	n/a
35	chr19:21540538-21540588	BJ	skin:	n/a
36	chr19:21541699-21541749	SKMC	muscle:	n/a
37	chr19:21541537-21541587	AG10803	skin:	n/a
38	chr19:21540536-21540586	HepG2	liver:	n/a
39	chr19:21541044-21541094	HEEpiC	esophagus:	n/a
40	chr19:21541772-21541822	HPAEpiC	pulmonary alveolar:	n/a
41	chr19:21513138-21513188	GM12878	blood:	n/a
42	chr19:21541772-21541822	AG04450	lung:	fetal
43	chr19:21541917-21541967	AG04449	skin:	fetal
44	chr19:21512166-21512216	SAEC	small airway:	n/a
45	chr19:21541537-21541587	LNCaP	prostate:	n/a
46	chr19:21541035-21541085	A549	lung:	n/a
47	chr19:21512378-21512428	HAEpiC	amniotic membrane:	n/a
48	chr19:21541772-21541822	SK-N-MC	brain:	n/a
49	chr19:21541793-21541843	SK-N-SH	brain:	n/a
50	chr19:21512202-21512252	Caco-2	colon:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21511427..21512224-chr9:140135317..140136194,2	Hela-S3	cervix:
2	chr19:21324747..21325334-chr19:21541551..21542092,2	Hela-S3	cervix:
3	chr19:21511256..21513599-chr19:21513725..21515814,2	MCF-7	breast:
4	chr19:21482877..21485011-chr19:21492555..21495180,2	K562	blood:
5	chr19:21552085..21554128-chr19:21570405..21572893,2	K562	blood:
6	chr19:21510924..21513197-chr19:21688433..21691004,2	MCF-7	breast:
7	chr19:21264733..21265247-chr19:21541544..21542206,2	NB4	blood:
8	chr19:21503005..21505616-chr19:21507489..21509547,2	K562	blood:
9	chr19:21496090..21497696-chr19:21505089..21507534,2	K562	blood:
10	chr19:21504637..21507576-chr19:21510636..21512879,2	MCF-7	breast:
11	chr19:21520831..21523621-chr19:21524615..21527542,2	K562	blood:
12	chr19:21501353..21503397-chr19:21510480..21512126,2	MCF-7	breast:
13	chr19:21509704..21512429-chr19:21517111..21519937,3	K562	blood:
14	chr19:21496090..21497696-chr19:21505089..21507534,2	K562	blood:
15	chr19:21501353..21503397-chr19:21510480..21512126,2	MCF-7	breast:
16	chr19:21520831..21523621-chr19:21524615..21527542,2	K562	blood:
17	chr19:21503005..21505616-chr19:21507489..21509547,2	K562	blood:
18	chr19:21500655..21502261-chr19:21504561..21506244,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF738-1	chr19:21558671-21558766	NR_027130
2	lnc-ZNF738-1	chr19:21558040-21558166	NR_027130
3	lnc-ZNF708-8	chr19:21562076-21562253	ucscGeneNc_uc002nqg_2
4	lnc-ZNF738-3	chr19:21500963-21501521	NONHSAT063699
5	lnc-ZNF708-8	chr19:21566420-21568648	ucscGeneNc_uc002nqg_2
6	lnc-ZNF708-7	chr19:21561505-21561885	ucscGeneNc_uc002nqe_1
7	lnc-ZNF738-1	chr19:21560191-21571384	NR_027130
8	lnc-ZNF708-7	chr19:21544979-21546181	ucscGeneNc_uc002nqe_1
9	lnc-ZNF738-1	chr19:21541735-21541945	NR_027130
10	lnc-ZNF708-6	chr19:21555198-21557246	ucscGeneNc_uc002nqf_1
11	lnc-ZNF738-1	chr19:21544568-21544660	NR_027130

No data

Variant related genes	Relation type
ENSG00000268322	TF binding region
ZNF738	TF binding region
ZNF708	TF binding region
ENSG00000268731	TF binding region
ENSG00000213976	TF binding region
ENSG00000268322	CpG island
ZNF738	CpG island
ZNF708	CpG island
ENSG00000268731	CpG island
ENSG00000213976	CpG island
ENSG00000160352	chromatin interactions
ENSG00000197013	chromatin interactions
ENSG00000268322	chromatin interactions
ENSG00000196705	chromatin interactions
ENSG00000182141	chromatin interactions
ENSG00000188229	chromatin interactions

Extended variants
information (count: 2605 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:2605 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376869459	chr19:21492006-21492007	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs368676662	chr19:21492010-21492011	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs2968064	chr19:21492012-21492013	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs373139290	chr19:21492020-21492021	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs541919680	chr19:21492031-21492032	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs2928193	chr19:21492032-21492033	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs200357549	chr19:21492045-21492046	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs140295887	chr19:21492048-21492049	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs547516	chr19:21492062-21492063	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs529406189	chr19:21492079-21492080	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs148002618	chr19:21492099-21492100	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs141649029	chr19:21492105-21492106	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs192863348	chr19:21492167-21492168	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs531704831	chr19:21492266-21492267	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111934050	chr19:21492275-21492276	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533645265	chr19:21492292-21492293	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185136182	chr19:21492312-21492313	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2992090	chr19:21492337-21492338	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139450392	chr19:21492341-21492342	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535261263	chr19:21492357-21492358	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374641868	chr19:21492441-21492442	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552039	chr19:21492504-21492505	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs564395982	chr19:21492518-21492519	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113091160	chr19:21492600-21492601	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369396796	chr19:21492688-21492689	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201845901	chr19:21492699-21492700	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114788316	chr19:21492722-21492723	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190067966	chr19:21492726-21492727	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201055234	chr19:21492765-21492766	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373043800	chr19:21492775-21492776	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192300240	chr19:21492792-21492793	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553902742	chr19:21492804-21492805	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184732156	chr19:21492811-21492812	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551615332	chr19:21492899-21492900	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558086462	chr19:21492942-21492943	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs670813	chr19:21492971-21492972	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs543827178	chr19:21493008-21493009	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146874409	chr19:21493019-21493020	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571596457	chr19:21493027-21493028	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188116135	chr19:21493046-21493047	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559859455	chr19:21493092-21493093	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11666026	chr19:21493101-21493102	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2968063	chr19:21493137-21493138	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181015626	chr19:21493205-21493206	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368336971	chr19:21493246-21493247	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372056271	chr19:21493255-21493256	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531144310	chr19:21493257-21493258	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs202120976	chr19:21493258-21493259	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144509553	chr19:21493260-21493261	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528948729	chr19:21493261-21493262	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2533 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21465000-21496000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr19:21473800-21510400	Weak transcription	Fetal Heart	heart
3	chr19:21474400-21492400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr19:21474800-21509800	Weak transcription	Fetal Brain Male	brain
5	chr19:21475200-21511200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:21476800-21497600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr19:21477000-21494400	Weak transcription	Stomach Mucosa	stomach
8	chr19:21477200-21495000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr19:21477600-21495800	Weak transcription	HepG2	liver
10	chr19:21478000-21497400	Weak transcription	Colon Smooth Muscle	Colon
11	chr19:21478200-21492600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr19:21478400-21500600	Weak transcription	Psoas Muscle	Psoas
13	chr19:21478600-21499200	Weak transcription	HMEC	breast
14	chr19:21481000-21500600	Weak transcription	NHLF	lung
15	chr19:21481200-21493000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
16	chr19:21481600-21500000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr19:21481600-21500400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr19:21481600-21505600	Weak transcription	K562	blood
19	chr19:21481800-21492600	Strong transcription	Fetal Muscle Leg	muscle
20	chr19:21481800-21493000	Strong transcription	Dnd41	blood
21	chr19:21481800-21493400	Strong transcription	Fetal Stomach	stomach
22	chr19:21482000-21492400	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr19:21482000-21493200	Strong transcription	Fetal Muscle Trunk	muscle
24	chr19:21482000-21493800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr19:21482400-21492800	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr19:21483200-21492800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr19:21483600-21493000	Strong transcription	Primary B cells from peripheral blood	blood
28	chr19:21484000-21492200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr19:21484200-21492200	Weak transcription	Rectal Smooth Muscle	rectum
30	chr19:21484200-21494200	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr19:21484400-21493200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr19:21484400-21511000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr19:21484600-21492400	Strong transcription	Fetal Intestine Large	intestine
34	chr19:21484800-21492000	Weak transcription	Brain Hippocampus Middle	brain
35	chr19:21485000-21493000	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr19:21485200-21494000	Weak transcription	NHDF-Ad	bronchial
37	chr19:21485200-21495000	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr19:21485400-21508600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr19:21485400-21511200	Weak transcription	Gastric	stomach
40	chr19:21485600-21497600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:21485600-21504200	Weak transcription	Pancreas	Pancrea
42	chr19:21486200-21492000	Weak transcription	Colonic Mucosa	Colon
43	chr19:21486200-21493000	Strong transcription	Duodenum Mucosa	Duodenum
44	chr19:21486400-21492000	Weak transcription	Brain Germinal Matrix	brain
45	chr19:21486400-21500400	Weak transcription	Spleen	Spleen
46	chr19:21487000-21492400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr19:21487000-21492400	Strong transcription	Thymus	Thymus
48	chr19:21487200-21492600	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr19:21487400-21492000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr19:21487400-21495200	Weak transcription	Brain Angular Gyrus	brain

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