Variant report

Variant	esv14420
Chromosome Location	chr6:58776769-58780132
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:138)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:138 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:135217803..135218666-chr6:58777553..58778353,2	MCF-7	breast:
2	chr6:58777707..58778511-chr6:61909313..61909813,2	MCF-7	breast:
3	chr17:56735441..56738187-chr6:58776197..58778735,2	MCF-7	breast:
4	chr4:44422694..44424195-chr6:58776128..58778515,2	MCF-7	breast:
5	chr22:32301912..32302764-chr6:58776740..58777661,2	MCF-7	breast:
6	chr3:90451070..90451591-chr6:58777113..58777718,3	MCF-7	breast:
7	chr1:181394037..181394570-chr6:58777372..58778132,2	MCF-7	breast:
8	chr3:16360548..16361058-chr6:58778316..58779058,2	MCF-7	breast:
9	chr6:58778318..58779144-chr9:130843661..130844171,2	MCF-7	breast:
10	chr17:56736044..56736561-chr6:58778407..58779097,2	MCF-7	breast:
11	chr6:58776120..58778273-chr8:145699925..145701982,2	MCF-7	breast:
12	chr17:79008190..79010769-chr6:58777233..58779265,2	MCF-7	breast:
13	chr22:21356184..21359058-chr6:58776120..58778924,2	MCF-7	breast:
14	chr20:45984506..45987023-chr6:58776231..58780015,3	MCF-7	breast:
15	chr6:58778243..58779030-chrX:61731310..61731811,2	MCF-7	breast:
16	chr6:58776812..58777737-chr8:48324823..48325324,2	MCF-7	breast:
17	chr11:58677524..58679024-chr6:58777164..58778728,2	K562	blood:
18	chr6:58776676..58777225-chr8:72532546..72533088,2	MCF-7	breast:
19	chr5:157496470..157497451-chr6:58776593..58777234,3	MCF-7	breast:
20	chr17:73716896..73718915-chr6:58776651..58778729,2	MCF-7	breast:
21	chr20:52238301..52240090-chr6:58777406..58779226,2	MCF-7	breast:
22	chr6:58777651..58778267-chr6:61909313..61909813,3	MCF-7	breast:
23	chr6:58775076..58778073-chr8:103250732..103252303,2	K562	blood:
24	chr6:58776657..58777247-chrX:136737324..136737914,2	MCF-7	breast:
25	chr16:19191197..19191940-chr6:58777386..58777915,2	MCF-7	breast:
26	chr14:19023553..19024073-chr6:58778553..58779079,2	MCF-7	breast:
27	chr6:27776232..27779951-chr6:58776955..58780402,3	MCF-7	breast:
28	chr1:44683359..44684029-chr6:58777311..58778221,2	MCF-7	breast:
29	chr14:77757334..77757890-chr6:58776828..58777663,2	MCF-7	breast:
30	chr17:56707619..56709303-chr6:58776177..58777680,2	MCF-7	breast:
31	chr6:58776637..58777632-chr8:18871298..18871912,2	HCT-116	colon:
32	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
33	chr3:90451069..90451589-chr6:58776919..58777844,3	MCF-7	breast:
34	chr17:57697051..57699517-chr6:58775454..58778452,2	MCF-7	breast:
35	chr17:46984708..46987154-chr6:58777011..58778755,2	MCF-7	breast:
36	chr17:57918618..57920889-chr6:58777178..58778919,2	MCF-7	breast:
37	chr10:90750069..90750688-chr6:58777473..58778220,2	Hela-S3	cervix:
38	chr16:73430630..73432387-chr6:58777761..58779339,2	MCF-7	breast:
39	chr12:38031911..38033432-chr6:58776341..58779018,2	MCF-7	breast:
40	chr1:110090644..110091238-chr6:58776881..58777871,2	MCF-7	breast:
41	chr1:121484489..121485231-chr6:58779321..58780005,2	MCF-7	breast:
42	chr20:17516282..17517977-chr6:58775914..58778767,2	MCF-7	breast:
43	chr1:9910788..9913768-chr6:58778329..58780695,2	MCF-7	breast:
44	chr11:75291642..75294590-chr6:58777397..58779135,2	MCF-7	breast:
45	chr17:62622662..62623234-chr6:58778443..58779436,2	MCF-7	breast:
46	chr20:46129644..46132043-chr6:58777544..58779139,2	MCF-7	breast:
47	chr20:62493089..62495109-chr6:58777340..58778920,2	MCF-7	breast:
48	chr18:73688396..73689210-chr6:58777841..58778684,2	MCF-7	breast:
49	chr12:6493660..6495635-chr6:58777646..58779181,2	MCF-7	breast:
50	chr6:58775915..58778901-chr8:144691705..144693500,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1866 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1866 , 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	rs4299853	chr6:58776770-58776771	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
2	rs28865617	chr6:58776774-58776775	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
3	rs7451409	chr6:58776775-58776776	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
4	rs7450733	chr6:58776776-58776777	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
5	rs28760944	chr6:58776779-58776780	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
6	rs28768095	chr6:58776780-58776781	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
7	rs56398250	chr6:58776781-58776782	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
8	rs9632508	chr6:58776782-58776783	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
9	rs28811328	chr6:58776783-58776784	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
10	rs4632921	chr6:58776784-58776785	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
11	rs4524641	chr6:58776785-58776786	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
12	rs28787436	chr6:58776786-58776787	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
13	rs28885514	chr6:58776787-58776788	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
14	rs9377759	chr6:58776788-58776789	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
15	rs12211546	chr6:58776789-58776790	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
16	rs4472381	chr6:58776792-58776793	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
17	rs60609069	chr6:58776793-58776794	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
18	rs4928543	chr6:58776794-58776795	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
19	rs9377935	chr6:58776795-58776796	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
20	rs9500459	chr6:58776796-58776797	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
21	rs4928544	chr6:58776798-58776799	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
22	rs4391286	chr6:58776799-58776800	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
23	rs28897452	chr6:58776800-58776801	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
24	rs9377937	chr6:58776801-58776802	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
25	rs4401693	chr6:58776802-58776803	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
26	rs4928545	chr6:58776803-58776804	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
27	rs28864470	chr6:58776805-58776806	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
28	rs61526475	chr6:58776806-58776807	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
29	rs9377760	chr6:58776807-58776808	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
30	rs28884938	chr6:58776808-58776809	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
31	rs4476855	chr6:58776809-58776810	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
32	rs28827479	chr6:58776810-58776811	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
33	rs9500461	chr6:58776811-58776812	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
34	rs28831980	chr6:58776812-58776813	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
35	rs7746929	chr6:58776813-58776814	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
36	rs4928547	chr6:58776815-58776816	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
37	rs9377939	chr6:58776816-58776817	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
38	rs4307197	chr6:58776817-58776818	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
39	rs9500462	chr6:58776819-58776820	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
40	rs4928349	chr6:58776820-58776821	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
41	rs9638020	chr6:58776821-58776822	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
42	rs28874350	chr6:58776822-58776823	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
43	rs9377761	chr6:58776823-58776824	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
44	rs4615419	chr6:58776824-58776825	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs59907465	chr6:58776825-58776826	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs4292554	chr6:58776826-58776827	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
47	rs9404801	chr6:58776827-58776828	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
48	rs4928549	chr6:58776828-58776829	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
49	rs9391469	chr6:58776829-58776830	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
50	rs28837423	chr6:58776831-58776832	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	19 gene(s)	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:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58773400-58779400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr6:58773400-58779400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:58773400-58779400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:58773400-58779400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
5	chr6:58773400-58779400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr6:58773400-58779400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr6:58773400-58779400	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr6:58773400-58779400	ZNF genes & repeats	Fetal Stomach	stomach
9	chr6:58773400-58779400	ZNF genes & repeats	Left Ventricle	heart
10	chr6:58773600-58779200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
11	chr6:58773600-58779400	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
12	chr6:58773600-58779400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr6:58773600-58779400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr6:58773600-58779400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr6:58773600-58779400	ZNF genes & repeats	Primary B cells from cord blood	blood
16	chr6:58773600-58779400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
17	chr6:58773600-58779400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:58773600-58779400	ZNF genes & repeats	Fetal Intestine Large	intestine
19	chr6:58776200-58779400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr6:58776400-58778200	ZNF genes & repeats	Brain Germinal Matrix	brain
21	chr6:58776400-58779200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr6:58776400-58779400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:58776400-58779400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
24	chr6:58776400-58779400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr6:58776400-58779400	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
26	chr6:58776400-58779400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
27	chr6:58776600-58776800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:58776600-58776800	Flanking Bivalent TSS/Enh	Right Atrium	heart
29	chr6:58776600-58776800	Flanking Bivalent TSS/Enh	HSMM	muscle
30	chr6:58776600-58777000	ZNF genes & repeats	HepG2	liver
31	chr6:58776600-58777200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:58776600-58777200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
33	chr6:58776600-58777200	Flanking Bivalent TSS/Enh	Osteobl	bone
34	chr6:58776600-58777400	Flanking Bivalent TSS/Enh	Pancreas	Pancrea
35	chr6:58776600-58777400	Flanking Bivalent TSS/Enh	HSMMtube	muscle
36	chr6:58776600-58777400	Flanking Bivalent TSS/Enh	NHLF	lung
37	chr6:58776600-58777600	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:58776600-58777600	Flanking Bivalent TSS/Enh	Right Ventricle	heart
39	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
40	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Primary T killer memory cells from peripheral blood	blood
41	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
42	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
43	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
44	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
45	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Pancreatic Islets	Pancreatic Islet
46	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
47	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
48	chr6:58776600-58777800	Flanking Bivalent TSS/Enh	Dnd41	blood
49	chr6:58776600-58778000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:58776600-58778000	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine

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