Variant report

Variant	nsv1059328
Chromosome Location	chr19:21691123-21775948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:358)
CpG islands
(count:427)
Chromatin interactive
region (count:11)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21756597-21757002	K562	blood:	n/a	n/a
2	ATF1	chr19:21756594-21757067	K562	blood:	n/a	n/a
3	ATF1	chr19:21775871-21777447	K562	blood:	n/a	n/a
4	ATF3	chr19:21756520-21757045	K562	blood:	n/a	n/a
5	BACH1	chr19:21775825-21776466	K562	blood:	n/a	n/a
6	BACH1	chr19:21769790-21769935	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr19:21693031-21693169	K562	blood:	n/a	n/a
8	BHLHE40	chr19:21748929-21749238	K562	blood:	n/a	chr19:21749052-21749073 chr19:21749056-21749069
9	BHLHE40	chr19:21775428-21777483	K562	blood:	n/a	n/a
10	BHLHE40	chr19:21756673-21757583	K562	blood:	n/a	n/a
11	CBX3	chr19:21775702-21776564	K562	blood:	n/a	n/a
12	CBX3	chr19:21702263-21702592	K562	blood:	n/a	n/a
13	CBX3	chr19:21702289-21702654	K562	blood:	n/a	n/a
14	CBX3	chr19:21756514-21757083	K562	blood:	n/a	n/a
15	CCNT2	chr19:21691185-21691385	K562	blood:	n/a	n/a
16	CCNT2	chr19:21775821-21776167	K562	blood:	n/a	n/a
17	CCNT2	chr19:21769328-21769513	K562	blood:	n/a	n/a
18	CEBPB	chr19:21756680-21757218	K562	blood:	n/a	n/a
19	CEBPB	chr19:21715804-21716043	K562	blood:	n/a	n/a
20	CEBPB	chr19:21750847-21750982	K562	blood:	n/a	n/a
21	CEBPB	chr19:21704019-21704348	HepG2	liver:	n/a	chr19:21704174-21704185
22	CEBPB	chr19:21740957-21741100	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr19:21750808-21751049	K562	blood:	n/a	n/a
24	CEBPB	chr19:21775847-21776313	K562	blood:	n/a	n/a
25	CEBPB	chr19:21704026-21704273	K562	blood:	n/a	chr19:21704174-21704185
26	CEBPB	chr19:21759510-21759606	K562	blood:	n/a	n/a
27	CEBPB	chr19:21756463-21757311	K562	blood:	n/a	n/a
28	CEBPB	chr19:21715858-21715920	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr19:21704035-21704303	A549	lung:	n/a	chr19:21704174-21704185
30	CEBPB	chr19:21704016-21704332	IMR90	lung:	n/a	chr19:21704174-21704185
31	CEBPB	chr19:21756603-21757299	K562	blood:	n/a	n/a
32	CEBPD	chr19:21691055-21691459	K562	blood:	n/a	n/a
33	CEBPZ	chr19:21702442-21702596	HepG2	liver:	n/a	n/a
34	CHD2	chr19:21769126-21769272	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr19:21752031-21752238	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr19:21756576-21757234	K562	blood:	n/a	n/a
37	CREB1	chr19:21756465-21757280	K562	blood:	n/a	n/a
38	CTCF	chr19:21757218-21757312	Lung_OC	lung:	n/a	n/a
39	CTCF	chr19:21764536-21764601	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr19:21771492-21771553	Lung_OC	lung:	n/a	n/a
41	CTCF	chr19:21691124-21691154	K562	blood:	n/a	n/a
42	CTCF	chr19:21753960-21754110	GM12865	blood:	n/a	n/a
43	CTCF	chr19:21722985-21723020	LNCaP	prostate:	n/a	n/a
44	CTCF	chr19:21702318-21702403	Lung_OC	lung:	n/a	n/a
45	CTCF	chr19:21732116-21732154	LNCaP	prostate:	n/a	n/a
46	CTCF	chr19:21764680-21764830	K562	blood:	n/a	n/a
47	CTCF	chr19:21764774-21764931	K562	blood:	n/a	n/a
48	CTCF	chr19:21742240-21742390	GM12870	blood:	n/a	n/a
49	CTCF	chr19:21712413-21712499	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr19:21730338-21730424	GM20000	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21767566-21767616	HAEpiC	amniotic membrane:	n/a
2	chr19:21769430-21769480	HUVEC	blood vessel:	n/a
3	chr19:21773418-21773468	HNPCEpiC	eye:	n/a
4	chr19:21769190-21769240	PANC-1	pancreas:	n/a
5	chr19:21769190-21769240	HL-60	blood:	n/a
6	chr19:21767566-21767616	HRCEpiC	kidney:	n/a
7	chr19:21769430-21769480	ProgFib	skin:	n/a
8	chr19:21773418-21773468	AG04450	lung:	fetal
9	chr19:21769430-21769480	K562	blood:	n/a
10	chr19:21766543-21766593	T-47D	breast:	n/a
11	chr19:21773418-21773468	BE2_C	brain:	n/a
12	chr19:21773418-21773468	HEK293	kidney:	embryo
13	chr19:21769430-21769480	AG10803	skin:	n/a
14	chr19:21769190-21769240	NB4	blood:	n/a
15	chr19:21769315-21769365	Jurkat	blood:	n/a
16	chr19:21769315-21769365	NHBE	bronchial:	n/a
17	chr19:21769190-21769240	LNCaP	prostate:	n/a
18	chr19:21769315-21769365	HRE	kidney:	n/a
19	chr19:21773418-21773468	AG09309	skin:	n/a
20	chr19:21766543-21766593	NH-A	brain:	n/a
21	chr19:21766543-21766593	LNCaP	prostate:	n/a
22	chr19:21769315-21769365	MCF10A-Er-Src	breast:	n/a
23	chr19:21773418-21773468	ECC-1	luminal epithelium:	n/a
24	chr19:21773418-21773468	HCT-116	colon:	n/a
25	chr19:21769315-21769365	SKMC	muscle:	n/a
26	chr19:21767566-21767616	Jurkat	blood:	n/a
27	chr19:21773418-21773468	AG10803	skin:	n/a
28	chr19:21767566-21767616	K562	blood:	n/a
29	chr19:21769315-21769365	HMEC	breast:	n/a
30	chr19:21769736-21769786	GM06990	blood:	n/a
31	chr19:21769190-21769240	IMR90	lung:	fetal
32	chr19:21767566-21767616	HCT-116	colon:	n/a
33	chr19:21767566-21767616	AG04449	skin:	fetal
34	chr19:21767566-21767616	NHDF-neo	bronchial:	n/a
35	chr19:21769315-21769365	PANC-1	pancreas:	n/a
36	chr19:21767566-21767616	MCF-7	breast:	n/a
37	chr19:21769736-21769786	HIPEpiC	eye:	n/a
38	chr19:21769315-21769365	AoSMC	blood vessel:	n/a
39	chr19:21769736-21769786	MCF10A-Er-Src	breast:	n/a
40	chr19:21767566-21767616	SK-N-SH_RA	brain:	n/a
41	chr19:21766543-21766593	NHDF-neo	bronchial:	n/a
42	chr19:21769430-21769480	Caco-2	colon:	n/a
43	chr19:21767566-21767616	HCPEpiC	choroid plexus:	n/a
44	chr19:21766543-21766593	SAEC	small airway:	n/a
45	chr19:21767566-21767616	IMR90	lung:	fetal
46	chr19:21769430-21769480	HCT-116	colon:	n/a
47	chr19:21773418-21773468	GM12878	blood:	n/a
48	chr19:21769315-21769365	Caco-2	colon:	n/a
49	chr19:21769315-21769365	NT2-D1	testis:	n/a
50	chr19:21769315-21769365	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
2	chr19:21691065..21693260-chr19:21696883..21699244,2	MCF-7	breast:
3	chr19:21687245..21689707-chr19:21740240..21743085,2	MCF-7	breast:
4	chr19:21687904..21690838-chr19:21705351..21707923,2	K562	blood:
5	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
6	chr19:21689678..21691656-chr19:21877431..21879636,2	K562	blood:
7	chr19:21691065..21693260-chr19:21696883..21699244,2	MCF-7	breast:
8	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
9	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:
10	chr19:21691580..21693623-chr19:22017806..22019839,2	MCF-7	breast:
11	chr19:21769231..21770804-chr19:21773382..21775361,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF100-3	chr19:21751906-21752048	XLOC_013263
2	lnc-ZNF100-2	chr19:21754050-21754341	NONHSAT063727
3	lnc-ZNF100-3	chr19:21748631-21748673	XLOC_013263
4	lnc-ZNF100-8	chr19:21763358-21765406	NONHSAT063728
5	lnc-ZNF100-3	chr19:21747057-21747283	XLOC_013263
6	lnc-ZNF100-2	chr19:21769665-21770045	ENSG00000249473
7	lnc-ZNF100-3	chr19:21737442-21737754	ENSG00000268081.1
8	lnc-ZNF100-1	chr19:21770314-21770413	NONHSAT063731
9	lnc-ZNF100-3	chr19:21751906-21752039	ENSG00000268081.1
10	lnc-ZNF100-2	chr19:21753624-21754341	ENSG00000268555.1
11	lnc-ZNF100-3	chr19:21744136-21747283	XLOC_013263
12	lnc-ZNF100-2	chr19:21769665-21770179	NONHSAT063726
13	lnc-ZNF100-2	chr19:21752904-21754341	NONHSAT063726
14	lnc-ZNF100-2	chr19:21753139-21754341	ENSG00000249473
15	lnc-ZNF100-2	chr19:21762538-21762616	NONHSAT063727
16	lnc-ZNF708-11	chr19:21704145-21704698	NONHSAT063722
17	lnc-ZNF100-2	chr19:21769665-21770124	ENSG00000268555.1

No data

Variant related genes	Relation type
ENSG00000268705	TF binding region
ZNF429	TF binding region
ENSG00000268081	TF binding region
ENSG00000268555	TF binding region
ENSG00000268705	CpG island
ZNF429	CpG island
ENSG00000268081	CpG island
ENSG00000268555	CpG island
ENSG00000268555	chromatin interactions
ENSG00000197013	chromatin interactions
ENSG00000198521	chromatin interactions

Extended variants
information (count: 4414 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:4414 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142997302	chr19:21691208-21691209	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370920938	chr19:21691212-21691213	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574889437	chr19:21691240-21691241	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535644333	chr19:21691251-21691252	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530188162	chr19:21691277-21691278	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2062564	chr19:21691399-21691400	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs150662541	chr19:21691428-21691429	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189111301	chr19:21691462-21691463	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34788876	chr19:21691502-21691503	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs398034252	chr19:21691513-21691514	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537822620	chr19:21691517-21691518	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552870707	chr19:21691518-21691519	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576759165	chr19:21691546-21691547	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139802735	chr19:21691550-21691551	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111968373	chr19:21691684-21691685	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs562426588	chr19:21691697-21691698	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181836725	chr19:21691724-21691725	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1984771	chr19:21691797-21691798	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs547901696	chr19:21691807-21691808	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530578653	chr19:21691811-21691812	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573196717	chr19:21691821-21691822	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74546848	chr19:21691836-21691837	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs534303030	chr19:21691846-21691847	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149790342	chr19:21691854-21691855	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552053567	chr19:21691874-21691875	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112061454	chr19:21691884-21691885	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568056516	chr19:21691908-21691909	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187215214	chr19:21691935-21691936	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531593962	chr19:21691959-21691960	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550178833	chr19:21691993-21691994	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568386095	chr19:21692009-21692010	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6511255	chr19:21692027-21692028	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs61115928	chr19:21692055-21692056	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs116791558	chr19:21692079-21692080	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534635109	chr19:21692086-21692087	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191968804	chr19:21692096-21692097	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558479951	chr19:21692097-21692098	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs576707328	chr19:21692143-21692144	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543839759	chr19:21692148-21692149	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556095452	chr19:21692166-21692167	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574363281	chr19:21692172-21692173	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182698738	chr19:21692173-21692174	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186011382	chr19:21692195-21692196	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144685969	chr19:21692235-21692236	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139831240	chr19:21692287-21692288	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564205699	chr19:21692335-21692336	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144523355	chr19:21692337-21692338	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201878817	chr19:21692363-21692364	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190182786	chr19:21692376-21692377	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs147863246	chr19:21692387-21692388	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21689200-21694200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:21689200-21702000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:21689200-21702000	Weak transcription	Stomach Mucosa	stomach
4	chr19:21689400-21691200	Enhancers	Primary T cells fromperipheralblood	blood
5	chr19:21689400-21691200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr19:21689400-21691200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr19:21689400-21691200	Enhancers	Colon Smooth Muscle	Colon
8	chr19:21689400-21691600	Weak transcription	Fetal Thymus	thymus
9	chr19:21689400-21691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr19:21689400-21693000	Weak transcription	Small Intestine	intestine
11	chr19:21689400-21693800	Weak transcription	NHLF	lung
12	chr19:21689400-21694800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr19:21689400-21695200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr19:21689400-21698400	Weak transcription	Placenta	Placenta
15	chr19:21689400-21701200	Weak transcription	HSMMtube	muscle
16	chr19:21689400-21701600	Weak transcription	Brain Substantia Nigra	brain
17	chr19:21689400-21701600	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr19:21689400-21702000	Weak transcription	Left Ventricle	heart
19	chr19:21689400-21702000	Weak transcription	Right Ventricle	heart
20	chr19:21689600-21691200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr19:21689600-21691400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr19:21689600-21691400	Enhancers	Brain Cingulate Gyrus	brain
23	chr19:21689600-21691600	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr19:21689600-21692400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr19:21689600-21692600	Weak transcription	Fetal Brain Male	brain
26	chr19:21689600-21692800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr19:21689600-21693000	Weak transcription	Rectal Smooth Muscle	rectum
28	chr19:21689600-21695000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr19:21689600-21700800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr19:21689600-21701400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr19:21689600-21701600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr19:21689600-21702000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr19:21689800-21691200	Transcr. at gene 5' and 3'	Dnd41	blood
34	chr19:21689800-21691400	Enhancers	Fetal Heart	heart
35	chr19:21689800-21691400	ZNF genes & repeats	HSMM	muscle
36	chr19:21689800-21692400	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr19:21689800-21693200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:21689800-21693400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr19:21689800-21694200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr19:21689800-21694800	Weak transcription	Fetal Muscle Trunk	muscle
41	chr19:21689800-21695000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr19:21689800-21695600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr19:21689800-21696600	Weak transcription	Brain Anterior Caudate	brain
44	chr19:21689800-21697800	Weak transcription	Psoas Muscle	Psoas
45	chr19:21690000-21691200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:21690000-21691200	Strong transcription	Fetal Muscle Leg	muscle
47	chr19:21690000-21691400	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr19:21690000-21691600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:21690000-21691600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr19:21690000-21692000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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