Variant report

Variant	esv16605
Chromosome Location	chr6:58773521-58780132
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:146)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:146 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:
2	chr2:135217803..135218666-chr6:58777553..58778353,2	MCF-7	breast:
3	chr14:19023553..19024073-chr6:58778553..58779079,2	MCF-7	breast:
4	chr6:58777390..58779179-chr6:133135024..133136911,2	MCF-7	breast:
5	chr11:66445363..66446008-chr6:58776703..58777356,2	MCF-7	breast:
6	chr20:52560026..52560620-chr6:58777219..58777738,2	MCF-7	breast:
7	chr14:77757334..77757890-chr6:58776828..58777663,2	MCF-7	breast:
8	chr20:45901715..45902477-chr6:58778556..58779159,2	MCF-7	breast:
9	chr22:21356184..21359058-chr6:58776120..58778924,2	MCF-7	breast:
10	chr6:27776232..27779951-chr6:58776955..58780402,3	MCF-7	breast:
11	chr12:38032931..38033431-chr6:58776879..58777388,2	MCF-7	breast:
12	chr20:52424572..52427398-chr6:58777006..58778744,2	MCF-7	breast:
13	chr3:90451070..90451591-chr6:58777113..58777718,3	MCF-7	breast:
14	chr11:58677524..58679024-chr6:58777164..58778728,2	K562	blood:
15	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:
16	chr22:32301912..32302764-chr6:58776740..58777661,2	MCF-7	breast:
17	chr17:57697051..57699517-chr6:58775454..58778452,2	MCF-7	breast:
18	chr20:52815826..52816411-chr6:58777180..58778164,2	MCF-7	breast:
19	chr17:79008190..79010769-chr6:58777233..58779265,2	MCF-7	breast:
20	chr20:46129644..46132043-chr6:58777544..58779139,2	MCF-7	breast:
21	chr11:75291642..75294590-chr6:58777397..58779135,2	MCF-7	breast:
22	chr16:73430630..73432387-chr6:58777761..58779339,2	MCF-7	breast:
23	chr2:219259923..219262856-chr6:58776591..58778942,2	MCF-7	breast:
24	chr12:38031932..38033432-chr6:58775709..58777615,2	MCF-7	breast:
25	chr14:70592691..70594528-chr6:58777109..58778754,2	MCF-7	breast:
26	chr6:58777416..58779792-chr6:77801547..77804072,2	MCF-7	breast:
27	chr20:19633644..19634334-chr6:58777686..58778513,2	MCF-7	breast:
28	chr14:98326171..98326823-chr6:58778365..58778943,2	MCF-7	breast:
29	chr6:58777333..58777900-chr8:122346827..122347447,2	MCF-7	breast:
30	chr19:35488627..35490321-chr6:58777408..58779728,2	MCF-7	breast:
31	chr6:27805995..27806602-chr6:58778107..58778767,2	MCF-7	breast:
32	chr1:44683359..44684029-chr6:58777311..58778221,2	MCF-7	breast:
33	chr17:62622662..62623234-chr6:58778443..58779436,2	MCF-7	breast:
34	chr2:109819769..109820303-chr6:58776869..58777442,2	MCF-7	breast:
35	chr1:181394037..181394570-chr6:58777372..58778132,2	MCF-7	breast:
36	chr17:57930610..57932922-chr6:58777438..58780644,3	MCF-7	breast:
37	chr12:6493660..6495635-chr6:58777646..58779181,2	MCF-7	breast:
38	chr6:58777651..58778267-chr6:61909313..61909813,3	MCF-7	breast:
39	chr20:60877312..60877975-chr6:58777171..58777835,2	MCF-7	breast:
40	chr6:58777220..58778210-chr6:119855510..119856349,2	MCF-7	breast:
41	chr3:90450072..90451589-chr6:58776092..58777719,4	MCF-7	breast:
42	chr12:7070831..7073502-chr6:58777307..58779204,2	MCF-7	breast:
43	chr12:80435495..80437852-chr6:58775102..58777367,2	MCF-7	breast:
44	chr17:57928094..57930742-chr6:58776120..58778676,4	MCF-7	breast:
45	chr6:58777993..58779849-chr8:94211437..94213575,2	MCF-7	breast:
46	chr17:57920709..57924714-chr6:58775095..58779071,5	MCF-7	breast:
47	chr6:58775915..58778901-chr8:144691705..144693500,2	MCF-7	breast:
48	chr20:52327864..52329489-chr6:58775870..58778258,2	MCF-7	breast:
49	chr6:58778318..58779144-chr9:130843661..130844171,2	MCF-7	breast:
50	chr6:58776812..58777737-chr8:48324823..48325324,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000207708	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000126749	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000184436	chromatin interactions
ENSG00000089351	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000230513	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000257084	chromatin interactions
ENSG00000175866	chromatin interactions
ENSG00000237080	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000212017	chromatin interactions
ENSG00000268858	chromatin interactions
ENSG00000206754	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000160325	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000255326	chromatin interactions
ENSG00000104524	chromatin interactions
ENSG00000111321	chromatin interactions
ENSG00000132470	chromatin interactions
ENSG00000173914	chromatin interactions
ENSG00000103528	chromatin interactions
ENSG00000026103	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000185158	chromatin interactions
ENSG00000168209	chromatin interactions
ENSG00000207713	chromatin interactions
ENSG00000159202	chromatin interactions
ENSG00000101407	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000140553	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000101413	chromatin interactions
ENSG00000183665	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000248278	chromatin interactions
ENSG00000141367	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000160973	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000226137	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000204272	chromatin interactions
ENSG00000171858	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000136997	chromatin interactions

Extended variants
information (count: 3071 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3071 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571534657	chr6:58773521-58773522	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs538921619	chr6:58773522-58773523	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs577522674	chr6:58773523-58773524	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs547742064	chr6:58773525-58773526	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs565879107	chr6:58773527-58773528	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
6	rs574709827	chr6:58773530-58773531	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
7	rs576771653	chr6:58773531-58773532	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
8	rs576090405	chr6:58773532-58773533	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs536612960	chr6:58773539-58773540	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs4355637	chr6:58773540-58773541	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs4413636	chr6:58773546-58773547	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs4512251	chr6:58773552-58773553	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs559663232	chr6:58773553-58773554	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs545694939	chr6:58773555-58773556	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs542416701	chr6:58773558-58773559	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs563605032	chr6:58773559-58773560	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs531052037	chr6:58773561-58773562	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs200455281	chr6:58773569-58773570	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs528543418	chr6:58773573-58773574	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs7453998	chr6:58773575-58773576	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs112633906	chr6:58773580-58773581	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs147627479	chr6:58773581-58773582	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs536013600	chr6:58773582-58773583	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs4636051	chr6:58773589-58773590	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs537133920	chr6:58773594-58773595	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs558258742	chr6:58773596-58773597	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs576424676	chr6:58773598-58773599	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs534354555	chr6:58773599-58773600	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs553209018	chr6:58773601-58773602	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs574816745	chr6:58773613-58773614	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs542026240	chr6:58773618-58773619	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs373140430	chr6:58773621-58773622	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs557517897	chr6:58773623-58773624	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs74793720	chr6:58773625-58773626	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs62412761	chr6:58773632-58773633	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs76363663	chr6:58773634-58773635	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575779905	chr6:58773637-58773638	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs374468856	chr6:58773638-58773639	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs564611915	chr6:58773641-58773642	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs56306819	chr6:58773642-58773643	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs62412762	chr6:58773650-58773651	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs79679176	chr6:58773652-58773653	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs74455408	chr6:58773654-58773655	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs74748619	chr6:58773655-58773656	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs62412763	chr6:58773657-58773658	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs540635577	chr6:58773661-58773662	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs4544941	chr6:58773667-58773668	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs559656546	chr6:58773669-58773670	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs112294987	chr6:58773670-58773671	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs530017169	chr6:58773678-58773679	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58769800-58773600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:58773400-58773600	Active TSS	Aorta	Aorta
3	chr6:58773400-58773600	Active TSS	Ovary	ovary
4	chr6:58773400-58773600	Active TSS	Psoas Muscle	Psoas
5	chr6:58773400-58774000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
6	chr6:58773400-58774000	Flanking Bivalent TSS/Enh	Hela-S3	cervix
7	chr6:58773400-58774800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:58773400-58774800	ZNF genes & repeats	Brain Hippocampus Middle	brain
9	chr6:58773400-58774800	ZNF genes & repeats	Colon Smooth Muscle	Colon
10	chr6:58773400-58774800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
11	chr6:58773400-58774800	ZNF genes & repeats	Fetal Lung	lung
12	chr6:58773400-58774800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
13	chr6:58773400-58774800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
14	chr6:58773400-58774800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
15	chr6:58773400-58774800	ZNF genes & repeats	GM12878-XiMat	blood
16	chr6:58773400-58774800	ZNF genes & repeats	HUVEC	blood vessel
17	chr6:58773400-58775000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
18	chr6:58773400-58775000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:58773400-58775000	ZNF genes & repeats	Brain Anterior Caudate	brain
20	chr6:58773400-58775000	ZNF genes & repeats	Brain Cingulate Gyrus	brain
21	chr6:58773400-58775000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:58773400-58775000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
23	chr6:58773400-58775000	ZNF genes & repeats	Dnd41	blood
24	chr6:58773400-58775200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:58773400-58775200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr6:58773400-58775200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
27	chr6:58773400-58775400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
28	chr6:58773400-58775400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
29	chr6:58773400-58775600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
30	chr6:58773400-58775600	ZNF genes & repeats	Liver	Liver
31	chr6:58773400-58775800	ZNF genes & repeats	HMEC	breast
32	chr6:58773400-58776000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:58773400-58776000	ZNF genes & repeats	NH-A	brain
34	chr6:58773400-58776200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:58773400-58776200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:58773400-58776400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:58773400-58776400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
38	chr6:58773400-58776600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
39	chr6:58773400-58776600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
40	chr6:58773400-58776600	ZNF genes & repeats	Gastric	stomach
41	chr6:58773400-58776600	ZNF genes & repeats	Small Intestine	intestine
42	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
43	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
46	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
48	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
49	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
50	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart

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