Variant report

Variant	nsv1056332
Chromosome Location	chr19:21746555-21807647
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:600)
CpG islands
(count:428)
Chromatin interactive
region (count:12)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21776657-21777194	K562	blood:	n/a	n/a
2	ARID3A	chr19:21786732-21786984	K562	blood:	n/a	n/a
3	ARID3A	chr19:21794774-21795815	K562	blood:	n/a	n/a
4	ARID3A	chr19:21756597-21757002	K562	blood:	n/a	n/a
5	ARID3A	chr19:21800652-21800945	K562	blood:	n/a	n/a
6	ARID3A	chr19:21784781-21786180	K562	blood:	n/a	n/a
7	ARID3A	chr19:21775949-21776229	K562	blood:	n/a	n/a
8	ATF1	chr19:21794941-21795310	K562	blood:	n/a	n/a
9	ATF1	chr19:21775871-21777447	K562	blood:	n/a	n/a
10	ATF1	chr19:21785628-21786402	K562	blood:	n/a	n/a
11	ATF1	chr19:21787782-21788023	K562	blood:	n/a	n/a
12	ATF1	chr19:21787263-21787316	K562	blood:	n/a	n/a
13	ATF1	chr19:21786629-21787040	K562	blood:	n/a	n/a
14	ATF1	chr19:21756594-21757067	K562	blood:	n/a	n/a
15	ATF3	chr19:21756520-21757045	K562	blood:	n/a	n/a
16	ATF3	chr19:21785653-21786139	K562	blood:	n/a	n/a
17	ATF3	chr19:21776694-21777184	K562	blood:	n/a	n/a
18	BACH1	chr19:21769790-21769935	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:21775825-21776466	K562	blood:	n/a	n/a
20	BACH1	chr19:21777662-21777846	K562	blood:	n/a	n/a
21	BACH1	chr19:21783750-21783899	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr19:21787072-21787360	GM12878	blood:	n/a	n/a
23	BHLHE40	chr19:21787118-21787259	GM12878	blood:	n/a	n/a
24	BHLHE40	chr19:21785683-21787434	K562	blood:	n/a	n/a
25	BHLHE40	chr19:21775428-21777483	K562	blood:	n/a	n/a
26	BHLHE40	chr19:21787777-21787977	K562	blood:	n/a	n/a
27	BHLHE40	chr19:21782352-21782391	K562	blood:	n/a	n/a
28	BHLHE40	chr19:21785096-21785106	K562	blood:	n/a	n/a
29	BHLHE40	chr19:21748929-21749238	K562	blood:	n/a	chr19:21749052-21749073 chr19:21749056-21749069
30	BHLHE40	chr19:21756673-21757583	K562	blood:	n/a	n/a
31	BHLHE40	chr19:21794738-21795143	K562	blood:	n/a	n/a
32	BRCA1	chr19:21787066-21787726	H1-hESC	embryonic stem cell:	n/a	n/a
33	CBX3	chr19:21785499-21786084	K562	blood:	n/a	n/a
34	CBX3	chr19:21785429-21785900	K562	blood:	n/a	n/a
35	CBX3	chr19:21776630-21777275	K562	blood:	n/a	n/a
36	CBX3	chr19:21756514-21757083	K562	blood:	n/a	n/a
37	CBX3	chr19:21775702-21776564	K562	blood:	n/a	n/a
38	CCNT2	chr19:21775821-21776167	K562	blood:	n/a	n/a
39	CCNT2	chr19:21785630-21786222	K562	blood:	n/a	n/a
40	CCNT2	chr19:21776451-21777013	K562	blood:	n/a	n/a
41	CCNT2	chr19:21800593-21800799	K562	blood:	n/a	n/a
42	CCNT2	chr19:21769328-21769513	K562	blood:	n/a	n/a
43	CCNT2	chr19:21795029-21795236	K562	blood:	n/a	n/a
44	CEBPB	chr19:21800745-21800806	K562	blood:	n/a	n/a
45	CEBPB	chr19:21785346-21785986	K562	blood:	n/a	n/a
46	CEBPB	chr19:21776793-21777722	IMR90	lung:	n/a	n/a
47	CEBPB	chr19:21779780-21780285	A549	lung:	n/a	n/a
48	CEBPB	chr19:21776359-21777781	K562	blood:	n/a	n/a
49	CEBPB	chr19:21787278-21787791	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr19:21779688-21780694	IMR90	lung:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21766543-21766593	HEK293	kidney:	embryo
2	chr19:21766543-21766593	HEK293	kidney:	embryo
3	chr19:21773418-21773468	K562	blood:	n/a
4	chr19:21769736-21769786	HAEpiC	amniotic membrane:	n/a
5	chr19:21769190-21769240	HCM	heart:	n/a
6	chr19:21769736-21769786	NB4	blood:	n/a
7	chr19:21769190-21769240	GM12878	blood:	n/a
8	chr19:21766543-21766593	ovcar-3	ovarian:	n/a
9	chr19:21766543-21766593	HAEpiC	amniotic membrane:	n/a
10	chr19:21769736-21769786	MCF-7	breast:	n/a
11	chr19:21769315-21769365	U87	brain:	n/a
12	chr19:21767566-21767616	GM12891	blood:	n/a
13	chr19:21769315-21769365	Hepatocyte	liver:	n/a
14	chr19:21769736-21769786	NT2-D1	testis:	n/a
15	chr19:21769190-21769240	AG04449	skin:	fetal
16	chr19:21769315-21769365	BE2_C	brain:	n/a
17	chr19:21766543-21766593	GM12878	blood:	n/a
18	chr19:21767566-21767616	HRCEpiC	kidney:	n/a
19	chr19:21769430-21769480	GM12878	blood:	n/a
20	chr19:21767566-21767616	MCF-7	breast:	n/a
21	chr19:21769736-21769786	H1-hESC	embryonic stem cell:	embryo
22	chr19:21766543-21766593	ECC-1	luminal epithelium:	n/a
23	chr19:21769315-21769365	HCM	heart:	n/a
24	chr19:21773418-21773468	NB4	blood:	n/a
25	chr19:21773418-21773468	SAEC	small airway:	n/a
26	chr19:21773418-21773468	PFSK-1	brain:	n/a
27	chr19:21769430-21769480	PANC-1	pancreas:	n/a
28	chr19:21769315-21769365	NHDF-neo	bronchial:	n/a
29	chr19:21769315-21769365	GM12878	blood:	n/a
30	chr19:21767566-21767616	HCM	heart:	n/a
31	chr19:21769190-21769240	HAEpiC	amniotic membrane:	n/a
32	chr19:21769190-21769240	Jurkat	blood:	n/a
33	chr19:21769736-21769786	SK-N-MC	brain:	n/a
34	chr19:21766543-21766593	GM12892	blood:	n/a
35	chr19:21773418-21773468	SK-N-MC	brain:	n/a
36	chr19:21769315-21769365	GM06990	blood:	n/a
37	chr19:21769190-21769240	Hela-S3	cervix:	n/a
38	chr19:21773418-21773468	HNPCEpiC	eye:	n/a
39	chr19:21766543-21766593	PFSK-1	brain:	n/a
40	chr19:21769190-21769240	GM12891	blood:	n/a
41	chr19:21769315-21769365	HepG2	liver:	n/a
42	chr19:21769736-21769786	NHDF-neo	bronchial:	n/a
43	chr19:21766543-21766593	SKMC	muscle:	n/a
44	chr19:21766543-21766593	BE2_C	brain:	n/a
45	chr19:21766543-21766593	HRPEpiC	eye:	n/a
46	chr19:21767566-21767616	HCF	heart:	n/a
47	chr19:21773418-21773468	SKMC	muscle:	n/a
48	chr19:21773418-21773468	HL-60	blood:	n/a
49	chr19:21766543-21766593	CMK	blood:	n/a
50	chr19:21767566-21767616	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
2	chr19:21788851..21790670-chr19:21793445..21795166,2	K562	blood:
3	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
4	chr19:21780063..21781970-chr19:21783251..21784988,3	K562	blood:
5	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
6	chr19:21769231..21770804-chr19:21773382..21775361,2	K562	blood:
7	chr19:21776789..21778695-chr19:21784881..21786729,2	K562	blood:
8	chr19:21784507..21786165-chr19:21795628..21798618,2	K562	blood:
9	chr19:21780063..21781970-chr19:21783251..21784988,3	K562	blood:
10	chr19:21788851..21790670-chr19:21793445..21795166,2	K562	blood:
11	chr19:21784507..21786165-chr19:21795628..21798618,2	K562	blood:
12	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF100-2	chr19:21754050-21754341	NONHSAT063727
2	lnc-ZNF100-8	chr19:21763358-21765406	NONHSAT063728
3	lnc-ZNF100-3	chr19:21747057-21747283	XLOC_013263
4	lnc-ZNF100-2	chr19:21753624-21754341	ENSG00000268555.1
5	lnc-ZNF100-3	chr19:21748631-21748673	XLOC_013263
6	lnc-ZNF100-3	chr19:21751906-21752039	ENSG00000268081.1
7	lnc-ZNF100-2	chr19:21769665-21770179	NONHSAT063726
8	lnc-ZNF429-2	chr19:21797286-21797405	XLOC_013007
9	lnc-ZNF100-1	chr19:21777228-21777430	ENSG00000268240.1
10	lnc-ZNF100-2	chr19:21769665-21770045	ENSG00000249473
11	lnc-ZNF100-3	chr19:21744136-21747283	XLOC_013263
12	lnc-ZNF100-3	chr19:21751906-21752048	XLOC_013263
13	lnc-ZNF100-1	chr19:21770314-21770413	NONHSAT063731
14	lnc-ZNF429-2	chr19:21780079-21780167	XLOC_013007
15	lnc-ZNF100-2	chr19:21753139-21754341	ENSG00000249473
16	lnc-ZNF100-1	chr19:21776485-21776704	NONHSAT063731
17	lnc-ZNF100-2	chr19:21762538-21762616	NONHSAT063727
18	lnc-ZNF100-1	chr19:21776487-21776720	ENSG00000268240.1
19	lnc-ZNF100-2	chr19:21752904-21754341	NONHSAT063726
20	lnc-ZNF100-2	chr19:21769665-21770124	ENSG00000268555.1

No data

Variant related genes	Relation type
ENSG00000268240	TF binding region
ENSG00000268081	TF binding region
ENSG00000268555	TF binding region
ENSG00000268240	CpG island
ENSG00000268081	CpG island
ENSG00000268555	CpG island
ENSG00000268555	chromatin interactions
ENSG00000268240	chromatin interactions

Extended variants
information (count: 3606 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:3606 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376661478	chr19:21746569-21746570	Enhancers ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs528833485	chr19:21746582-21746583	Enhancers ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs75414941	chr19:21746585-21746586	Enhancers ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs547377301	chr19:21746586-21746587	Enhancers ZNF genes & repeats Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs559172126	chr19:21746632-21746633	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs73023895	chr19:21746645-21746646	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs76745657	chr19:21746677-21746678	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs115560647	chr19:21746678-21746679	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs371380854	chr19:21746709-21746710	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs73023898	chr19:21746723-21746724	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs73929311	chr19:21746747-21746748	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs533094379	chr19:21746748-21746749	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs73023899	chr19:21746755-21746756	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs539064106	chr19:21746765-21746766	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs80331924	chr19:21746786-21746787	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs73023902	chr19:21746798-21746799	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs200762608	chr19:21746808-21746809	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs112965467	chr19:21746815-21746816	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs202172475	chr19:21746837-21746838	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs200837344	chr19:21746846-21746847	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs201577246	chr19:21746870-21746871	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs199935914	chr19:21746876-21746877	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs75280480	chr19:21746935-21746936	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs572792978	chr19:21746965-21746966	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs201311904	chr19:21746967-21746968	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs142457126	chr19:21746972-21746973	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs530642442	chr19:21746988-21746989	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs139740465	chr19:21747008-21747009	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs567561023	chr19:21747023-21747024	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs534700064	chr19:21747051-21747052	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs553380201	chr19:21747056-21747057	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
32	rs571629657	chr19:21747057-21747058	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
33	rs539168463	chr19:21747117-21747118	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
34	rs185588690	chr19:21747145-21747146	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
35	rs566313726	chr19:21747146-21747147	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
36	rs575878593	chr19:21747166-21747167	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
37	rs190302769	chr19:21747173-21747174	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs182972605	chr19:21747178-21747179	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
39	rs187606573	chr19:21747207-21747208	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs535116608	chr19:21747214-21747215	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs540665013	chr19:21747228-21747229	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs145254667	chr19:21747229-21747230	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs191946845	chr19:21747243-21747244	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs558015906	chr19:21747286-21747287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74975845	chr19:21747299-21747300	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544677995	chr19:21747327-21747328	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563049534	chr19:21747337-21747338	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs202155396	chr19:21747347-21747348	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147605833	chr19:21747410-21747411	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548806706	chr19:21747417-21747418	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD

Chromatin state (count:1330 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21737200-21747200	ZNF genes & repeats	Fetal Intestine Small	intestine
2	chr19:21738000-21749400	Weak transcription	Left Ventricle	heart
3	chr19:21738000-21751400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr19:21738600-21751600	Weak transcription	Osteobl	bone
5	chr19:21739400-21751200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr19:21740600-21750600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr19:21742800-21750600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:21743200-21750400	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr19:21743600-21751600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr19:21744200-21747000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
11	chr19:21744800-21746600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:21744800-21747600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr19:21744800-21750600	Weak transcription	Colonic Mucosa	Colon
14	chr19:21744800-21750600	Weak transcription	Fetal Kidney	kidney
15	chr19:21745000-21750600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr19:21745200-21746600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr19:21745200-21749400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr19:21745800-21746800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr19:21745800-21747200	Strong transcription	Fetal Stomach	stomach
20	chr19:21745800-21748000	Strong transcription	Dnd41	blood
21	chr19:21746000-21746600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr19:21746000-21746600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr19:21746000-21746600	Strong transcription	Adipose Nuclei	Adipose
24	chr19:21746000-21746600	ZNF genes & repeats	Fetal Brain Male	brain
25	chr19:21746000-21746600	ZNF genes & repeats	Lung	lung
26	chr19:21746000-21746600	ZNF genes & repeats	Ovary	ovary
27	chr19:21746000-21746600	Strong transcription	Stomach Smooth Muscle	stomach
28	chr19:21746000-21746800	ZNF genes & repeats	Liver	Liver
29	chr19:21746000-21746800	Strong transcription	Fetal Lung	lung
30	chr19:21746000-21746800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
31	chr19:21746000-21747000	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr19:21746000-21747600	Strong transcription	Primary T cells from cord blood	blood
33	chr19:21746200-21746600	ZNF genes & repeats	Brain Germinal Matrix	brain
34	chr19:21746200-21746600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
35	chr19:21746200-21746600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
36	chr19:21746200-21746800	Strong transcription	Primary B cells from peripheral blood	blood
37	chr19:21746200-21746800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
38	chr19:21746200-21747000	ZNF genes & repeats	Thymus	Thymus
39	chr19:21746400-21746600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:21746400-21746600	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
41	chr19:21746400-21746600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:21746400-21747000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:21746400-21747000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
44	chr19:21746400-21747000	Strong transcription	Fetal Intestine Large	intestine
45	chr19:21746600-21746800	Strong transcription	Ovary	ovary
46	chr19:21746600-21747000	Weak transcription	NHDF-Ad	bronchial
47	chr19:21746600-21747200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:21746600-21748200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr19:21746600-21748400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr19:21746600-21749000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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