Variant report

Variant	nsv543948
Chromosome Location	chr19:21763457-21775948
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:428)
Chromatin interactive
region (count:3)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:21775871-21777447	K562	blood:	n/a	n/a
2	BACH1	chr19:21775825-21776466	K562	blood:	n/a	n/a
3	BACH1	chr19:21769790-21769935	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr19:21775428-21777483	K562	blood:	n/a	n/a
5	CBX3	chr19:21775702-21776564	K562	blood:	n/a	n/a
6	CCNT2	chr19:21775821-21776167	K562	blood:	n/a	n/a
7	CCNT2	chr19:21769328-21769513	K562	blood:	n/a	n/a
8	CEBPB	chr19:21775847-21776313	K562	blood:	n/a	n/a
9	CHD2	chr19:21769126-21769272	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr19:21764774-21764931	K562	blood:	n/a	n/a
11	CTCF	chr19:21764680-21764830	K562	blood:	n/a	n/a
12	CTCF	chr19:21764536-21764601	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr19:21771492-21771553	Lung_OC	lung:	n/a	n/a
14	CTCF	chr19:21769200-21769350	NHEK	skin:	n/a	n/a
15	CUX1	chr19:21775937-21777361	K562	blood:	n/a	n/a
16	ELF1	chr19:21773276-21773521	K562	blood:	n/a	chr19:21773376-21773389
17	EP300	chr19:21775773-21777330	K562	blood:	n/a	n/a
18	GABPA	chr19:21769154-21769791	H1-hESC	embryonic stem cell:	n/a	n/a
19	GATA2	chr19:21775722-21776253	K562	blood:	n/a	n/a
20	HMGN3	chr19:21775542-21776204	K562	blood:	n/a	n/a
21	IRF1	chr19:21775832-21776318	K562	blood:	n/a	n/a
22	IRF1	chr19:21774562-21774857	K562	blood:	n/a	n/a
23	IRF1	chr19:21774481-21774706	K562	blood:	n/a	n/a
24	JUND	chr19:21773868-21773905	K562	blood:	n/a	n/a
25	JUND	chr19:21769258-21769269	H1-hESC	embryonic stem cell:	n/a	n/a
26	JUND	chr19:21775737-21777346	K562	blood:	n/a	n/a
27	KAP1	chr19:21763487-21763781	K562	blood:	n/a	n/a
28	MAFF	chr19:21775843-21776334	K562	blood:	n/a	n/a
29	MAFF	chr19:21774459-21774534	HepG2	liver:	n/a	chr19:21774501-21774519
30	MAFF	chr19:21774485-21774683	K562	blood:	n/a	chr19:21774501-21774519
31	MAFK	chr19:21775798-21777301	K562	blood:	n/a	n/a
32	MAFK	chr19:21774364-21774571	HepG2	liver:	n/a	n/a
33	MAFK	chr19:21774478-21774636	K562	blood:	n/a	n/a
34	MAFK	chr19:21772795-21772825	K562	blood:	n/a	n/a
35	MAX	chr19:21775900-21776471	K562	blood:	n/a	n/a
36	MAX	chr19:21770859-21771214	K562	blood:	n/a	chr19:21770998-21771005 chr19:21771029-21771040 chr19:21771030-21771040 chr19:21771030-21771039 chr19:21771103-21771112 chr19:21771029-21771040 chr19:21770997-21771007
37	MAX	chr19:21770922-21771281	H1-hESC	embryonic stem cell:	n/a	chr19:21770998-21771005 chr19:21771029-21771040 chr19:21771030-21771040 chr19:21771030-21771039 chr19:21771103-21771112 chr19:21771029-21771040 chr19:21770997-21771007
38	MAX	chr19:21770865-21771208	A549	lung:	n/a	chr19:21770998-21771005 chr19:21771029-21771040 chr19:21771103-21771112 chr19:21771030-21771040 chr19:21771030-21771039 chr19:21771029-21771040 chr19:21770997-21771007
39	MAX	chr19:21775681-21776245	K562	blood:	n/a	n/a
40	MAZ	chr19:21775575-21777375	K562	blood:	n/a	n/a
41	MXI1	chr19:21769076-21769117	H1-hESC	embryonic stem cell:	n/a	n/a
42	MYC	chr19:21775734-21777260	K562	blood:	n/a	n/a
43	MYC	chr19:21766334-21766464	MCF-7	breast:	n/a	chr19:21766439-21766450
44	NR2F2	chr19:21775728-21776346	K562	blood:	n/a	n/a
45	NR2F2	chr19:21775801-21776188	K562	blood:	n/a	n/a
46	POLR2A	chr19:21769002-21771379	PBDE	blood:	n/a	n/a
47	POLR2A	chr19:21766366-21766447	MCF-7	breast:	n/a	n/a
48	POLR2A	chr19:21775628-21775991	K562	blood:	n/a	n/a
49	POLR2A	chr19:21766345-21766442	MCF-7	breast:	n/a	n/a
50	POLR2A	chr19:21771086-21771120	MCF-7	breast:	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	chr19:21769190-21769240	PrEC	prostate:	n/a
2	chr19:21769190-21769240	PrEC	prostate:	n/a
3	chr19:21767566-21767616	PrEC	prostate:	n/a
4	chr19:21773418-21773468	HUVEC	blood vessel:	n/a
5	chr19:21769315-21769365	SKMC	muscle:	n/a
6	chr19:21767566-21767616	ovcar-3	ovarian:	n/a
7	chr19:21767566-21767616	HepG2	liver:	n/a
8	chr19:21773418-21773468	U87	brain:	n/a
9	chr19:21769736-21769786	PrEC	prostate:	n/a
10	chr19:21769736-21769786	HL-60	blood:	n/a
11	chr19:21773418-21773468	HCT-116	colon:	n/a
12	chr19:21766543-21766593	U87	brain:	n/a
13	chr19:21769430-21769480	HRCEpiC	kidney:	n/a
14	chr19:21769736-21769786	MCF10A-Er-Src	breast:	n/a
15	chr19:21769190-21769240	RPTEC	kidney:	n/a
16	chr19:21769430-21769480	HCF	heart:	n/a
17	chr19:21769736-21769786	NHBE	bronchial:	n/a
18	chr19:21769315-21769365	U87	brain:	n/a
19	chr19:21769315-21769365	HUVEC	blood vessel:	n/a
20	chr19:21769315-21769365	SAEC	small airway:	n/a
21	chr19:21769430-21769480	Caco-2	colon:	n/a
22	chr19:21766543-21766593	HIPEpiC	eye:	n/a
23	chr19:21769736-21769786	HCT-116	colon:	n/a
24	chr19:21766543-21766593	GM12878	blood:	n/a
25	chr19:21767566-21767616	K562	blood:	n/a
26	chr19:21767566-21767616	GM12892	blood:	n/a
27	chr19:21766543-21766593	HPAEpiC	pulmonary alveolar:	n/a
28	chr19:21767566-21767616	HPAEpiC	pulmonary alveolar:	n/a
29	chr19:21769736-21769786	ProgFib	skin:	n/a
30	chr19:21769315-21769365	GM19239	blood:	n/a
31	chr19:21773418-21773468	CMK	blood:	n/a
32	chr19:21769430-21769480	HMEC	breast:	n/a
33	chr19:21766543-21766593	HMEC	breast:	n/a
34	chr19:21769315-21769365	AoSMC	blood vessel:	n/a
35	chr19:21773418-21773468	NHDF-neo	bronchial:	n/a
36	chr19:21773418-21773468	Hepatocyte	liver:	n/a
37	chr19:21769315-21769365	SK-N-MC	brain:	n/a
38	chr19:21769430-21769480	Hepatocyte	liver:	n/a
39	chr19:21766543-21766593	IMR90	lung:	fetal
40	chr19:21769190-21769240	HAEpiC	amniotic membrane:	n/a
41	chr19:21767566-21767616	NHDF-neo	bronchial:	n/a
42	chr19:21769190-21769240	GM19239	blood:	n/a
43	chr19:21769736-21769786	NT2-D1	testis:	n/a
44	chr19:21767566-21767616	CMK	blood:	n/a
45	chr19:21769736-21769786	HMEC	breast:	n/a
46	chr19:21767566-21767616	ECC-1	luminal epithelium:	n/a
47	chr19:21769190-21769240	SKMC	muscle:	n/a
48	chr19:21766543-21766593	AoSMC	blood vessel:	n/a
49	chr19:21769190-21769240	NB4	blood:	n/a
50	chr19:21767566-21767616	SAEC	small airway:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21769231..21770804-chr19:21773382..21775361,2	K562	blood:
2	chr19:21757543..21760677-chr19:21760984..21764499,3	K562	blood:
3	chr19:21759399..21762531-chr19:21766206..21768542,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF100-2	chr19:21769665-21770179	NONHSAT063726
2	lnc-ZNF100-2	chr19:21769665-21770045	ENSG00000249473
3	lnc-ZNF100-2	chr19:21769665-21770124	ENSG00000268555.1
4	lnc-ZNF100-8	chr19:21763358-21765406	NONHSAT063728
5	lnc-ZNF100-1	chr19:21770314-21770413	NONHSAT063731

No data

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

Extended variants
information (count: 565 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567818867	chr19:21763539-21763540	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
2	rs145820426	chr19:21763540-21763541	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
3	rs369842185	chr19:21763544-21763545	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
4	rs368227710	chr19:21763602-21763603	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
5	rs535273872	chr19:21763628-21763629	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
6	rs78049066	chr19:21763686-21763687	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
7	rs553624795	chr19:21763708-21763709	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
8	rs571872906	chr19:21763724-21763725	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
9	rs551483526	chr19:21763731-21763732	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
10	rs377727743	chr19:21763747-21763748	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
11	rs571392688	chr19:21763757-21763758	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
12	rs527264412	chr19:21763788-21763789	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
13	rs146935668	chr19:21763797-21763798	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
14	rs543070637	chr19:21763832-21763833	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs55963311	chr19:21763870-21763871	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs34455476	chr19:21763873-21763874	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs547383856	chr19:21763889-21763890	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs35752041	chr19:21763896-21763897	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs117849782	chr19:21763914-21763915	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs540915637	chr19:21763927-21763928	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs11878379	chr19:21763986-21763987	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533110768	chr19:21764027-21764028	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs115151995	chr19:21764073-21764074	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs141626774	chr19:21764126-21764127	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs530938031	chr19:21764179-21764180	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs371976537	chr19:21764240-21764241	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs570222307	chr19:21764302-21764303	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs549488381	chr19:21764305-21764306	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs35523768	chr19:21764333-21764334	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs186064423	chr19:21764359-21764360	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs371811035	chr19:21764384-21764385	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs528673404	chr19:21764395-21764396	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs374830388	chr19:21764416-21764417	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
34	rs73552442	chr19:21764429-21764430	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs11881858	chr19:21764469-21764470	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
36	rs73027768	chr19:21764543-21764544	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
37	rs538938700	chr19:21764637-21764638	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
38	rs557640022	chr19:21764649-21764650	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
39	rs542606782	chr19:21764650-21764651	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
40	rs536691853	chr19:21764658-21764659	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
41	rs183156799	chr19:21764677-21764678	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
42	rs555042106	chr19:21764687-21764688	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
43	rs35595475	chr19:21764736-21764737	ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs187198613	chr19:21764802-21764803	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
45	rs113778978	chr19:21764831-21764832	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
46	rs190446787	chr19:21764843-21764844	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
47	rs73027770	chr19:21764865-21764866	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs538475877	chr19:21764895-21764896	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
49	rs544933937	chr19:21764921-21764922	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
50	rs375738787	chr19:21764961-21764962	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:38)

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

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21752000-21769600	Weak transcription	Fetal Heart	heart
2	chr19:21752800-21766200	Weak transcription	Fetal Intestine Large	intestine
3	chr19:21753000-21768000	Weak transcription	Fetal Intestine Small	intestine
4	chr19:21757000-21764400	Weak transcription	Pancreas	Pancrea
5	chr19:21759400-21764600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr19:21760200-21768000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:21760400-21769000	Weak transcription	Fetal Kidney	kidney
8	chr19:21762200-21764000	Enhancers	Primary T cells from cord blood	blood
9	chr19:21762200-21765000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr19:21762400-21763800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr19:21762400-21764000	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr19:21762600-21766800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr19:21763200-21763800	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr19:21763200-21763800	Transcr. at gene 5' and 3'	Dnd41	blood
15	chr19:21763200-21764400	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr19:21763400-21764600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr19:21763400-21767200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:21763400-21767400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr19:21763400-21768000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr19:21763800-21764200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr19:21763800-21764400	Genic enhancers	Dnd41	blood
22	chr19:21764000-21767400	Weak transcription	Primary T cells from cord blood	blood
23	chr19:21764000-21767400	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr19:21764200-21765000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr19:21764400-21765200	Enhancers	Pancreas	Pancrea
26	chr19:21764400-21765600	Transcr. at gene 5' and 3'	Dnd41	blood
27	chr19:21764400-21767600	Enhancers	Primary T cells fromperipheralblood	blood
28	chr19:21764600-21764800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:21764600-21764800	Enhancers	Gastric	stomach
30	chr19:21764600-21768000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr19:21764800-21766200	Weak transcription	Gastric	stomach
32	chr19:21764800-21769000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:21765000-21767200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr19:21765200-21766200	Weak transcription	Pancreas	Pancrea
35	chr19:21765600-21766200	Genic enhancers	Dnd41	blood
36	chr19:21766200-21766400	ZNF genes & repeats	Brain Anterior Caudate	brain
37	chr19:21766200-21766400	ZNF genes & repeats	Gastric	stomach
38	chr19:21766200-21766600	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
39	chr19:21766200-21766600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
40	chr19:21766200-21766600	ZNF genes & repeats	Lung	lung
41	chr19:21766200-21766600	ZNF genes & repeats	Pancreas	Pancrea
42	chr19:21766200-21766600	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
43	chr19:21766200-21766600	ZNF genes & repeats	Rectal Smooth Muscle	rectum
44	chr19:21766200-21766600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
45	chr19:21766200-21766800	Strong transcription	Fetal Intestine Large	intestine
46	chr19:21766200-21766800	ZNF genes & repeats	Left Ventricle	heart
47	chr19:21766200-21767000	Transcr. at gene 5' and 3'	Dnd41	blood
48	chr19:21766200-21770600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr19:21766600-21767600	Weak transcription	Pancreas	Pancrea
50	chr19:21766600-21768000	Weak transcription	Rectal Mucosa Donor 31	rectum

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