Variant report

Variant	esv3435793
Chromosome Location	chr19:27732650-27739215
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:90)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:28193921..28196192-chr19:27738694..27740822,2	MCF-7	breast:
2	chr17:58603504..58604171-chr19:27738843..27739764,2	MCF-7	breast:
3	chr17:59482833..59484547-chr19:27731694..27733523,2	MCF-7	breast:
4	chr19:27731229..27733515-chr19:27737682..27740212,3	MCF-7	breast:
5	chr19:27738271..27740312-chr4:68262912..68265515,2	MCF-7	breast:
6	chr19:27734776..27735283-chr4:142678250..142679232,2	MCF-7	breast:
7	chr19:27738249..27739002-chr7:18865984..18866492,2	MCF-7	breast:
8	chr19:27730503..27733214-chr19:27735926..27737745,2	K562	blood:
9	chr1:121484264..121485397-chr19:27732209..27732850,5	K562	blood:
10	chr10:42528302..42530981-chr19:27731210..27733512,2	MCF-7	breast:
11	chr19:27738271..27739820-chr6:58772163..58774918,2	MCF-7	breast:
12	chr1:121482889..121485426-chr19:27733290..27740540,17	K562	blood:
13	chr19:27732330..27733194-chr5:176074096..176074934,2	Hela-S3	cervix:
14	chr10:42527520..42529802-chr19:27732626..27735592,2	K562	blood:
15	chr1:121482676..121485402-chr19:27730501..27733214,12	K562	blood:
16	chr10:42528075..42531081-chr19:27735905..27739791,6	MCF-7	breast:
17	chr11:117787369..117787889-chr19:27738686..27739368,2	K562	blood:
18	chr17:19335400..19335900-chr19:27733012..27733518,2	MCF-7	breast:
19	chr19:18498589..18499092-chr19:27739098..27739794,2	HCT-116	colon:
20	chr10:42528106..42531063-chr19:27736683..27739174,2	K562	blood:
21	chr19:27731229..27733214-chr8:102884050..102885632,2	MCF-7	breast:
22	chr1:121484518..121485402-chr19:27734128..27734629,2	K562	blood:
23	chr1:121484518..121485426-chr19:27732227..27733212,7	MCF-7	breast:
24	chr19:27732230..27732731-chr8:18696335..18696835,2	MCF-7	breast:
25	chr10:71897930..71900730-chr19:27730502..27732728,2	MCF-7	breast:
26	chr1:121483890..121484451-chr19:27736926..27737426,2	MCF-7	breast:
27	chr10:42526475..42528192-chr19:27731227..27733212,2	MCF-7	breast:
28	chr12:34844445..34846343-chr19:27735903..27737749,2	K562	blood:
29	chr19:27732209..27732712-chr2:133011942..133012867,2	MCF-7	breast:
30	chr1:121482889..121485426-chr19:27735763..27740540,17	K562	blood:
31	chr19:27736247..27738846-chr8:34200775..34202275,2	MCF-7	breast:
32	chr19:27730503..27732709-chr9:139305201..139307172,2	MCF-7	breast:
33	chr17:56707857..56709514-chr19:27731768..27734278,2	MCF-7	breast:
34	chr16:69363397..69365027-chr19:27738551..27740871,2	MCF-7	breast:
35	chr19:27731258..27733523-chr2:232326492..232328767,2	MCF-7	breast:
36	chr19:27731229..27733515-chr19:27737682..27740212,3	MCF-7	breast:
37	chr19:27732227..27733066-chr2:112641278..112641778,2	NB4	blood:
38	chr17:57921146..57922788-chr19:27733727..27736557,3	MCF-7	breast:
39	chr10:42532112..42532613-chr19:27734969..27735848,2	MCF-7	breast:
40	chr1:121484536..121485417-chr19:27732233..27733219,3	MCF-7	breast:
41	chr19:27732023..27732712-chr20:46012477..46013112,2	MCF-7	breast:
42	chr1:121483185..121485419-chr19:27730521..27734410,16	K562	blood:
43	chr19:27738249..27739165-chr3:64009126..64009721,2	MCF-7	breast:
44	chr12:34844846..34846346-chr19:27731700..27733247,2	MCF-7	breast:
45	chr19:27738500..27739360-chr2:237227769..237228539,2	MCF-7	breast:
46	chr18:60172493..60172994-chr19:27739182..27739818,2	MCF-7	breast:
47	chr1:121483138..121485425-chr19:27735007..27739872,9	MCF-7	breast:
48	chr14:31781406..31781906-chr19:27732227..27733066,2	MCF-7	breast:
49	chr1:149214587..149215555-chr19:27732071..27732710,2	NB4	blood:
50	chr19:27732167..27734609-chr5:14472438..14475218,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000163636	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000267959	chromatin interactions
ENSG00000258429	chromatin interactions
ENSG00000048140	chromatin interactions
ENSG00000062725	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000153107	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000051108	chromatin interactions
ENSG00000252826	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000259349	chromatin interactions
ENSG00000198105	chromatin interactions
ENSG00000186184	chromatin interactions
ENSG00000115053	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000038382	chromatin interactions
ENSG00000139517	chromatin interactions
ENSG00000180573	chromatin interactions

Extended variants
information (count: 2091 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:2091 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200888265	chr19:27732661-27732662	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs577939212	chr19:27732662-27732663	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs77451260	chr19:27732663-27732664	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs2177878	chr19:27732665-27732666	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs4352169	chr19:27732670-27732671	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs538917420	chr19:27732674-27732675	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs2177879	chr19:27732675-27732676	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs9710612	chr19:27732682-27732683	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs557330767	chr19:27732683-27732684	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs200856860	chr19:27732689-27732690	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs576498587	chr19:27732691-27732692	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs9710614	chr19:27732692-27732693	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs543762167	chr19:27732694-27732695	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs200032240	chr19:27732697-27732698	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs561957239	chr19:27732701-27732702	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs574054101	chr19:27732712-27732713	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs541196145	chr19:27732720-27732721	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs79796046	chr19:27732726-27732727	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs559506582	chr19:27732732-27732733	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs12980336	chr19:27732733-27732734	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs78292947	chr19:27732734-27732735	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs12980337	chr19:27732737-27732738	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs7408488	chr19:27732741-27732742	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs78884233	chr19:27732756-27732757	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs533389935	chr19:27732760-27732761	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs545293753	chr19:27732761-27732762	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs563593054	chr19:27732764-27732765	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs531119991	chr19:27732765-27732766	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs548928437	chr19:27732767-27732768	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs567170803	chr19:27732768-27732769	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs201748158	chr19:27732772-27732773	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs528166812	chr19:27732776-27732777	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs372248051	chr19:27732787-27732788	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs79903355	chr19:27732809-27732810	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs62136070	chr19:27732812-27732813	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs62136071	chr19:27732813-27732814	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs538879763	chr19:27732819-27732820	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs62136072	chr19:27732826-27732827	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs62136073	chr19:27732829-27732830	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs557205960	chr19:27732831-27732832	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs62136074	chr19:27732832-27732833	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs536179923	chr19:27732833-27732834	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs555712560	chr19:27732837-27732838	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs573986331	chr19:27732838-27732839	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs541118419	chr19:27732841-27732842	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs553098696	chr19:27732845-27732846	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs577719236	chr19:27732850-27732851	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs376849892	chr19:27732853-27732854	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs369406768	chr19:27732854-27732855	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs545156821	chr19:27732856-27732857	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	11 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:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:27731800-27733000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
2	chr19:27731800-27733000	ZNF genes & repeats	Fetal Kidney	kidney
3	chr19:27731800-27733000	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
4	chr19:27731800-27733400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:27731800-27733400	Flanking Bivalent TSS/Enh	Aorta	Aorta
6	chr19:27731800-27733400	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
7	chr19:27731800-27733400	ZNF genes & repeats	Right Ventricle	heart
8	chr19:27731800-27733400	Flanking Bivalent TSS/Enh	NH-A	brain
9	chr19:27731800-27733400	ZNF genes & repeats	NHEK	skin
10	chr19:27731800-27733600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
11	chr19:27731800-27733600	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr19:27731800-27733600	Flanking Bivalent TSS/Enh	Gastric	stomach
13	chr19:27731800-27733600	Flanking Bivalent TSS/Enh	Hela-S3	cervix
14	chr19:27731800-27734600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:27731800-27734600	ZNF genes & repeats	Brain Germinal Matrix	brain
16	chr19:27731800-27734600	ZNF genes & repeats	Placenta	Placenta
17	chr19:27731800-27734800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr19:27731800-27734800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:27731800-27734800	ZNF genes & repeats	Esophagus	oesophagus
20	chr19:27731800-27734800	ZNF genes & repeats	Pancreas	Pancrea
21	chr19:27731800-27734800	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
22	chr19:27731800-27734800	ZNF genes & repeats	GM12878-XiMat	blood
23	chr19:27731800-27735000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr19:27731800-27735000	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
25	chr19:27731800-27735000	ZNF genes & repeats	Fetal Brain Female	brain
26	chr19:27731800-27735400	ZNF genes & repeats	Fetal Thymus	thymus
27	chr19:27731800-27736200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
28	chr19:27731800-27737000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
29	chr19:27731800-27737000	ZNF genes & repeats	Osteobl	bone
30	chr19:27731800-27738600	ZNF genes & repeats	Thymus	Thymus
31	chr19:27731800-27739000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
32	chr19:27731800-27739600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
33	chr19:27731800-27739600	ZNF genes & repeats	Brain Hippocampus Middle	brain
34	chr19:27731800-27739600	ZNF genes & repeats	Fetal Intestine Large	intestine
35	chr19:27731800-27739600	ZNF genes & repeats	Ovary	ovary
36	chr19:27731800-27739600	ZNF genes & repeats	Spleen	Spleen
37	chr19:27731800-27739800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr19:27731800-27739800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
39	chr19:27731800-27739800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
40	chr19:27731800-27739800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr19:27731800-27739800	ZNF genes & repeats	Fetal Stomach	stomach
42	chr19:27731800-27740000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
43	chr19:27731800-27740000	ZNF genes & repeats	Colonic Mucosa	Colon
44	chr19:27731800-27740200	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr19:27731800-27740400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr19:27731800-27740400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr19:27731800-27740400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr19:27731800-27740400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr19:27731800-27740400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
50	chr19:27731800-27740400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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