Variant report

Variant	nsv2470
Chromosome Location	chr19:35655281-35702565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:70)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:35654052..35658593-chr19:35736953..35742683,9	K562	blood:
2	chr19:35644439..35646610-chr19:35662548..35664453,2	MCF-7	breast:
3	chr19:35691908..35694570-chr19:35738700..35740998,2	K562	blood:
4	chr19:35653735..35656865-chr19:35656931..35659382,3	MCF-7	breast:
5	chr19:35700181..35702948-chr19:35738888..35740935,3	MCF-7	breast:
6	chr19:35666862..35669002-chr19:35676994..35679868,2	K562	blood:
7	chr19:35681330..35684144-chr19:35686479..35687982,2	K562	blood:
8	chr19:35699017..35701710-chr19:35704867..35706681,2	K562	blood:
9	chr19:35656275..35658757-chr19:35668459..35673698,5	K562	blood:
10	chr19:35666862..35669002-chr19:35676994..35679868,2	K562	blood:
11	chr19:35680181..35681833-chr19:35683643..35685960,2	K562	blood:
12	chr19:35652170..35655595-chr19:35655947..35659208,4	MCF-7	breast:
13	chr19:35676990..35679771-chr19:35683266..35685850,2	K562	blood:
14	chr19:35659165..35661294-chr19:35670153..35671780,2	K562	blood:
15	chr19:35699735..35702638-chr19:35738803..35741415,2	K562	blood:
16	chr19:35688259..35691483-chr19:35738721..35741363,4	MCF-7	breast:
17	chr19:35658586..35660197-chr19:35739044..35740712,2	K562	blood:
18	chr19:35653699..35655552-chr19:35738412..35739992,2	K562	blood:
19	chr19:35606015..35607604-chr19:35656192..35659125,2	MCF-7	breast:
20	chr19:35653833..35655711-chr19:35656998..35660022,4	K562	blood:
21	chr19:35659935..35661487-chr19:35664872..35667024,2	K562	blood:
22	chr19:35658448..35660082-chr19:35706961..35709327,2	K562	blood:
23	chr19:35681330..35684144-chr19:35686479..35687982,2	K562	blood:
24	chr19:35659935..35661487-chr19:35664872..35667024,2	K562	blood:
25	chr19:35688853..35690621-chr19:35737302..35739922,2	MCF-7	breast:
26	chr19:35660384..35663163-chr19:35664605..35666174,2	MCF-7	breast:
27	chr19:35653961..35659020-chr19:35755691..35760689,8	K562	blood:
28	chr19:35659165..35661294-chr19:35670153..35671780,2	K562	blood:
29	chr19:35670858..35673817-chr19:35687638..35690435,2	K562	blood:
30	chr19:35670858..35673817-chr19:35687638..35690435,2	K562	blood:
31	chr19:35659935..35661802-chr19:35663380..35667024,3	K562	blood:
32	chr19:35680181..35681833-chr19:35683643..35685960,2	K562	blood:
33	chr19:35657732..35659414-chr19:35738597..35740391,2	MCF-7	breast:
34	chr19:35676990..35679771-chr19:35683266..35685850,2	K562	blood:
35	chr19:35690573..35693790-chr19:35694961..35698637,4	K562	blood:
36	chr19:35642928..35645381-chr19:35657672..35659375,2	MCF-7	breast:
37	chr19:35660634..35663962-chr19:35667353..35669168,3	K562	blood:
38	chr19:35653961..35658211-chr19:35756444..35760028,4	K562	blood:
39	chr19:35656896..35658640-chr19:35739040..35741411,2	MCF-7	breast:
40	chr19:35659935..35661802-chr19:35663380..35667024,3	K562	blood:
41	chr19:35662152..35664028-chr19:35739883..35742034,2	K562	blood:
42	chr19:35699047..35700792-chr19:35711759..35713606,2	MCF-7	breast:
43	chr19:35655231..35657834-chr19:35695851..35698454,2	MCF-7	breast:
44	chr19:35658538..35660564-chr19:35760467..35762500,2	K562	blood:
45	chr19:35669103..35671214-chr19:35737457..35739938,2	K562	blood:
46	chr19:35686366..35688378-chr19:35693649..35696328,2	K562	blood:
47	chr19:35689192..35690781-chr19:35710324..35712969,2	K562	blood:
48	chr19:35689748..35692688-chr19:35698548..35701014,3	K562	blood:
49	chr19:35656275..35658757-chr19:35668459..35673698,5	K562	blood:
50	chr19:35662646..35664738-chr19:35675000..35677629,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LSR-1	chr19:35701776-35701887	XLOC_013049
2	lnc-LSR-1	chr19:35697056-35697295	XLOC_013049
3	lnc-FXYD7-2	chr19:35657154-35657228	NR_028406
4	lnc-FAM187B-1	chr19:35695381-35695670	uc_449_-
5	lnc-FXYD7-2	chr19:35657045-35657074	NR_028406
6	lnc-FXYD7-2	chr19:35660469-35660788	NR_028406
7	lnc-LSR-1	chr19:35696059-35696179	XLOC_013049
8	lnc-LSR-1	chr19:35697707-35697729	NONHSAT065812
9	lnc-LSR-1	chr19:35697056-35697295	XLOC_013049
10	lnc-FXYD5-1	chr19:35695381-35695670	uc_449_+
11	lnc-LSR-1	chr19:35696059-35696179	XLOC_013049
12	lnc-LSR-1	chr19:35695955-35696179	XLOC_013049

No data

Variant related genes	Relation type
ENSG00000089327	chromatin interactions
ENSG00000089356	chromatin interactions
ENSG00000105698	chromatin interactions
ENSG00000105697	chromatin interactions
ENSG00000105699	chromatin interactions
TMEM184B	miRNA target sites

Extended variants
information (count: 1871 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1871 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73588893	chr19:35655289-35655290	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559514493	chr19:35655308-35655309	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs572825128	chr19:35655317-35655318	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs73044017	chr19:35655345-35655346	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs537717288	chr19:35655354-35655355	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs565008763	chr19:35655372-35655373	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs56347218	chr19:35655472-35655473	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs78794409	chr19:35655595-35655596	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142911323	chr19:35655603-35655604	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs370340402	chr19:35655685-35655686	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184557945	chr19:35655755-35655756	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs549279950	chr19:35655840-35655841	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566239736	chr19:35655875-35655876	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs552544616	chr19:35655892-35655893	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367612789	chr19:35655907-35655908	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201420598	chr19:35655986-35655987	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs386808898	chr19:35655988-35655989	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs534920273	chr19:35655989-35655990	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs56058408	chr19:35655990-35655991	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs571452751	chr19:35656024-35656025	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs192867513	chr19:35656025-35656026	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs185790464	chr19:35656075-35656076	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs573819738	chr19:35656108-35656109	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs536571402	chr19:35656147-35656148	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs553021526	chr19:35656172-35656173	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs1688008	chr19:35656183-35656184	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs545265698	chr19:35656245-35656246	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs1672995	chr19:35656246-35656247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs575417115	chr19:35656254-35656255	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs531544244	chr19:35656270-35656271	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs544190556	chr19:35656318-35656319	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs545421383	chr19:35656329-35656330	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs375293902	chr19:35656330-35656331	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs113673493	chr19:35656338-35656339	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs560957578	chr19:35656385-35656386	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs190267465	chr19:35656396-35656397	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs564269366	chr19:35656404-35656405	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs543287653	chr19:35656412-35656413	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs113050356	chr19:35656490-35656491	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs180965545	chr19:35656546-35656547	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs551561670	chr19:35656604-35656605	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs113906794	chr19:35656643-35656644	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs571365589	chr19:35656658-35656659	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs530927675	chr19:35656745-35656746	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs143910362	chr19:35656748-35656749	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs372400233	chr19:35656778-35656779	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs376987895	chr19:35656792-35656793	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs183484158	chr19:35656828-35656829	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs188555817	chr19:35656862-35656863	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs181325494	chr19:35656905-35656906	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	18160780	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35646600-35656800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:35647800-35657000	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr19:35648000-35661600	Strong transcription	H1 Cell Line	embryonic stem cell
4	chr19:35648000-35661800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr19:35648200-35656600	Strong transcription	Fetal Thymus	thymus
6	chr19:35648200-35662800	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr19:35648400-35657000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr19:35649200-35657000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr19:35649400-35656400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr19:35649400-35656800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:35649400-35657400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
12	chr19:35650000-35656600	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr19:35650400-35655800	Strong transcription	Duodenum Mucosa	Duodenum
14	chr19:35650600-35655400	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr19:35650800-35656600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
16	chr19:35651800-35657000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
17	chr19:35651800-35657000	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr19:35652000-35657400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr19:35652000-35657600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
20	chr19:35652000-35661800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
21	chr19:35652200-35655600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr19:35652200-35657800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr19:35652200-35657800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
24	chr19:35652200-35658000	ZNF genes & repeats	GM12878-XiMat	blood
25	chr19:35652200-35658200	ZNF genes & repeats	A549	lung
26	chr19:35652400-35655600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
27	chr19:35652400-35655600	ZNF genes & repeats	Aorta	Aorta
28	chr19:35652400-35655600	ZNF genes & repeats	Left Ventricle	heart
29	chr19:35652400-35655600	ZNF genes & repeats	HSMM	muscle
30	chr19:35652400-35656200	ZNF genes & repeats	NH-A	brain
31	chr19:35652400-35657400	ZNF genes & repeats	Primary B cells from cord blood	blood
32	chr19:35652400-35657800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr19:35652400-35658400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
34	chr19:35652400-35658400	ZNF genes & repeats	Lung	lung
35	chr19:35652400-35658600	ZNF genes & repeats	Placenta	Placenta
36	chr19:35652600-35657400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr19:35652800-35656600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr19:35653000-35656800	Genic enhancers	K562	blood
39	chr19:35653000-35658000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
40	chr19:35653200-35656400	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr19:35653200-35658000	ZNF genes & repeats	HMEC	breast
42	chr19:35653400-35655600	Strong transcription	Rectal Smooth Muscle	rectum
43	chr19:35653400-35657400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr19:35653400-35657600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr19:35653400-35658000	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr19:35653400-35663800	Weak transcription	Stomach Mucosa	stomach
47	chr19:35653600-35655600	ZNF genes & repeats	NHDF-Ad	bronchial
48	chr19:35653600-35655800	ZNF genes & repeats	HUVEC	blood vessel
49	chr19:35653600-35657000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr19:35653600-35658000	ZNF genes & repeats	Osteobl	bone

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