Variant report

Variant	esv3347460
Chromosome Location	chr19:27733072-27762365
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:81)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:57931756..57934704-chr19:27735828..27738481,2	MCF-7	breast:
2	chr1:121483051..121485429-chr19:27736244..27740196,9	MCF-7	breast:
3	chr1:121482654..121485417-chr19:27730386..27733214,11	MCF-7	breast:
4	chr12:34844825..34846346-chr19:27731692..27733219,2	K562	blood:
5	chr19:27732231..27733220-chr8:18696335..18696835,2	MCF-7	breast:
6	chr19:27738249..27739165-chr3:64009126..64009721,2	MCF-7	breast:
7	chr19:27732330..27733194-chr5:176074096..176074934,2	Hela-S3	cervix:
8	chr10:42528106..42531063-chr19:27736683..27739174,2	K562	blood:
9	chr19:27733264..27735341-chr5:49544077..49545577,2	MCF-7	breast:
10	chr1:121483185..121485419-chr19:27730521..27734410,16	K562	blood:
11	chr19:27730503..27733214-chr19:27735926..27737745,2	K562	blood:
12	chr19:27735092..27735592-chr4:68265165..68265924,2	MCF-7	breast:
13	chr1:12392654..12393407-chr19:27738850..27739687,2	MCF-7	breast:
14	chr12:28945509..28947009-chr19:27732727..27734566,2	MCF-7	breast:
15	chr17:56707857..56709514-chr19:27731768..27734278,2	MCF-7	breast:
16	chr17:59482833..59484547-chr19:27731694..27733523,2	MCF-7	breast:
17	chr19:27731258..27733523-chr2:232326492..232328767,2	MCF-7	breast:
18	chr12:34844846..34846346-chr19:27731700..27733247,2	MCF-7	breast:
19	chr19:27731227..27733512-chr20:55840170..55842696,2	MCF-7	breast:
20	chr1:121482889..121485426-chr19:27735763..27740540,17	K562	blood:
21	chr19:18390431..18393009-chr19:27731584..27734229,2	MCF-7	breast:
22	chr10:42528436..42531081-chr19:27736662..27739367,4	MCF-7	breast:
23	chr17:19335400..19335900-chr19:27733012..27733518,2	MCF-7	breast:
24	chr12:34844445..34846343-chr19:27735903..27737749,2	K562	blood:
25	chr16:5710936..5711647-chr19:27738832..27739454,2	MCF-7	breast:
26	chr19:18498589..18499092-chr19:27739098..27739794,2	HCT-116	colon:
27	chr1:121484518..121485402-chr19:27734128..27734629,2	K562	blood:
28	chr1:121482889..121485426-chr19:27733290..27740540,17	K562	blood:
29	chr19:27738500..27739360-chr2:237227769..237228539,2	MCF-7	breast:
30	chr1:121484242..121485223-chr19:27739792..27740312,2	MCF-7	breast:
31	chr10:42526475..42528192-chr19:27731227..27733212,2	MCF-7	breast:
32	chr10:42529302..42529920-chr19:27734982..27735519,2	MCF-7	breast:
33	chr19:27731229..27733515-chr19:27737682..27740212,3	MCF-7	breast:
34	chr1:121483052..121485434-chr19:27730501..27733191,4	MCF-7	breast:
35	chr17:57921146..57922788-chr19:27733727..27736557,3	MCF-7	breast:
36	chr19:27731229..27733214-chr8:102884050..102885632,2	MCF-7	breast:
37	chr16:69363397..69365027-chr19:27738551..27740871,2	MCF-7	breast:
38	chr10:42528302..42530981-chr19:27731210..27733512,2	MCF-7	breast:
39	chr1:121482676..121485402-chr19:27730501..27733214,12	K562	blood:
40	chr17:58603504..58604171-chr19:27738843..27739764,2	MCF-7	breast:
41	chr1:121483138..121485425-chr19:27735007..27739872,9	MCF-7	breast:
42	chr10:42397869..42400416-chr19:27731046..27733513,2	MCF-7	breast:
43	chr13:28193921..28196192-chr19:27738694..27740822,2	MCF-7	breast:
44	chr1:121484705..121485205-chr19:27733910..27734629,2	MCF-7	breast:
45	chr1:121484523..121485419-chr19:27732208..27733212,6	MCF-7	breast:
46	chr1:121483890..121484451-chr19:27736926..27737426,2	MCF-7	breast:
47	chr10:42529082..42529941-chr19:27738664..27739193,3	MCF-7	breast:
48	chr10:42529415..42529944-chr19:27739260..27739782,2	MCF-7	breast:
49	chr10:42530126..42531081-chr19:27738662..27739344,3	MCF-7	breast:
50	chr19:27731712..27733212-chr19:27736249..27738480,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000130522	chromatin interactions
ENSG00000186184	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000048140	chromatin interactions
ENSG00000062725	chromatin interactions
ENSG00000267959	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000139517	chromatin interactions
ENSG00000258429	chromatin interactions
ENSG00000259349	chromatin interactions
ENSG00000115053	chromatin interactions
ENSG00000038382	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000177238	chromatin interactions

Extended variants
information (count: 5227 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:5227 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536395885	chr19:27733073-27733074	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs555152190	chr19:27733074-27733075	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs74217686	chr19:27733077-27733078	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs140265667	chr19:27733081-27733082	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs573552511	chr19:27733084-27733085	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs369210206	chr19:27733085-27733086	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs540957572	chr19:27733087-27733088	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs371284173	chr19:27733095-27733096	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs375388723	chr19:27733098-27733099	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs576956649	chr19:27733107-27733108	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs544294055	chr19:27733108-27733109	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs201857363	chr19:27733109-27733110	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs375837556	chr19:27733111-27733112	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs8113262	chr19:27733112-27733113	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs560316745	chr19:27733114-27733115	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs199868358	chr19:27733117-27733118	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs527559130	chr19:27733118-27733119	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs552085919	chr19:27733123-27733124	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs373380789	chr19:27733126-27733127	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs201065844	chr19:27733130-27733131	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs571296376	chr19:27733132-27733133	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs202125173	chr19:27733134-27733135	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs78109071	chr19:27733135-27733136	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs538692413	chr19:27733137-27733138	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs201982825	chr19:27733139-27733140	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs569210144	chr19:27733141-27733142	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs536776792	chr19:27733142-27733143	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs554845304	chr19:27733143-27733144	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs567107077	chr19:27733146-27733147	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs140679439	chr19:27733152-27733153	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs369444370	chr19:27733157-27733158	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs373390632	chr19:27733158-27733159	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs534488720	chr19:27733159-27733160	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs8108606	chr19:27733171-27733172	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs78050377	chr19:27733172-27733173	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs577617356	chr19:27733176-27733177	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs543820543	chr19:27733179-27733180	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs556140643	chr19:27733180-27733181	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs8108695	chr19:27733183-27733184	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs78066345	chr19:27733187-27733188	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs74809126	chr19:27733190-27733191	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs541937189	chr19:27733194-27733195	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs559898600	chr19:27733196-27733197	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs376370441	chr19:27733199-27733200	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs149646380	chr19:27733201-27733202	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs370407404	chr19:27733202-27733203	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs373822770	chr19:27733208-27733209	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs71181463	chr19:27733209-27733210	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs377383595	chr19:27733211-27733212	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs545686785	chr19:27733216-27733217	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:38)

Disease	PMID	Source
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	21248843	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	19287141	CNVD
Lung cancer	18438408	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:27731800-27733400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:27731800-27733400	Flanking Bivalent TSS/Enh	Aorta	Aorta
3	chr19:27731800-27733400	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
4	chr19:27731800-27733400	ZNF genes & repeats	Right Ventricle	heart
5	chr19:27731800-27733400	Flanking Bivalent TSS/Enh	NH-A	brain
6	chr19:27731800-27733400	ZNF genes & repeats	NHEK	skin
7	chr19:27731800-27733600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
8	chr19:27731800-27733600	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr19:27731800-27733600	Flanking Bivalent TSS/Enh	Gastric	stomach
10	chr19:27731800-27733600	Flanking Bivalent TSS/Enh	Hela-S3	cervix
11	chr19:27731800-27734600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr19:27731800-27734600	ZNF genes & repeats	Brain Germinal Matrix	brain
13	chr19:27731800-27734600	ZNF genes & repeats	Placenta	Placenta
14	chr19:27731800-27734800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:27731800-27734800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr19:27731800-27734800	ZNF genes & repeats	Esophagus	oesophagus
17	chr19:27731800-27734800	ZNF genes & repeats	Pancreas	Pancrea
18	chr19:27731800-27734800	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
19	chr19:27731800-27734800	ZNF genes & repeats	GM12878-XiMat	blood
20	chr19:27731800-27735000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr19:27731800-27735000	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
22	chr19:27731800-27735000	ZNF genes & repeats	Fetal Brain Female	brain
23	chr19:27731800-27735400	ZNF genes & repeats	Fetal Thymus	thymus
24	chr19:27731800-27736200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
25	chr19:27731800-27737000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:27731800-27737000	ZNF genes & repeats	Osteobl	bone
27	chr19:27731800-27738600	ZNF genes & repeats	Thymus	Thymus
28	chr19:27731800-27739000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chr19:27731800-27739600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
30	chr19:27731800-27739600	ZNF genes & repeats	Brain Hippocampus Middle	brain
31	chr19:27731800-27739600	ZNF genes & repeats	Fetal Intestine Large	intestine
32	chr19:27731800-27739600	ZNF genes & repeats	Ovary	ovary
33	chr19:27731800-27739600	ZNF genes & repeats	Spleen	Spleen
34	chr19:27731800-27739800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr19:27731800-27739800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
36	chr19:27731800-27739800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
37	chr19:27731800-27739800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr19:27731800-27739800	ZNF genes & repeats	Fetal Stomach	stomach
39	chr19:27731800-27740000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
40	chr19:27731800-27740000	ZNF genes & repeats	Colonic Mucosa	Colon
41	chr19:27731800-27740200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr19:27731800-27740400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr19:27731800-27740400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr19:27731800-27740400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr19:27731800-27740400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr19:27731800-27740400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
47	chr19:27731800-27740400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:27731800-27740400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
49	chr19:27731800-27740400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
50	chr19:27731800-27740400	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood

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