Variant report

Variant	nsv546851
Chromosome Location	chr1:94916649-94941376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:255)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94929310-94929611	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:94937794-94938064	IMR90	lung:	n/a	chr1:94937930-94937943
3	CTCF	chr1:94929256-94929664	GM12878	blood:	n/a	n/a
4	CTCF	chr1:94929380-94929530	AG09319	gingival:	n/a	n/a
5	CTCF	chr1:94929360-94929510	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr1:94929380-94929530	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr1:94929361-94929528	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr1:94929380-94929530	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr1:94929400-94929550	HMF	breast:	n/a	n/a
10	CTCF	chr1:94929300-94929579	K562	blood:	n/a	n/a
11	CTCF	chr1:94929370-94929573	GM13977	blood:	n/a	n/a
12	CTCF	chr1:94929380-94929530	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr1:94929440-94929590	GM12864	blood:	n/a	n/a
14	CTCF	chr1:94929380-94929530	SAEC	small airway:	n/a	n/a
15	CTCF	chr1:94929299-94929614	K562	blood:	n/a	n/a
16	CTCF	chr1:94929440-94929590	HEK293	kidney:	n/a	n/a
17	CTCF	chr1:94929360-94929510	AG04450	lung:	n/a	n/a
18	CTCF	chr1:94929420-94929570	HRE	kidney:	n/a	n/a
19	CTCF	chr1:94929400-94929550	GM12873	blood:	n/a	n/a
20	CTCF	chr1:94929360-94929510	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr1:94929360-94929510	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr1:94929440-94929590	Caco-2	colon:	n/a	n/a
23	CTCF	chr1:94929390-94929569	A549	lung:	n/a	n/a
24	CTCF	chr1:94929300-94929450	NHEK	skin:	n/a	n/a
25	CTCF	chr1:94929460-94929610	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:94929355-94929564	LNCaP	prostate:	n/a	n/a
27	CTCF	chr1:94929380-94929530	HEK293	kidney:	n/a	n/a
28	CTCF	chr1:94929360-94929510	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr1:94929347-94929589	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:94929420-94929570	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr1:94929295-94929552	T-47D	breast:	n/a	n/a
32	CTCF	chr1:94929380-94929530	BE2_C	brain:	n/a	n/a
33	CTCF	chr1:94929349-94929580	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr1:94929380-94929530	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:94929380-94929530	HRE	kidney:	n/a	n/a
36	CTCF	chr1:94929360-94929510	BE2_C	brain:	n/a	n/a
37	CTCF	chr1:94929520-94929670	A549	lung:	n/a	n/a
38	CTCF	chr1:94929393-94929554	Fibrobl	skin:	n/a	n/a
39	CTCF	chr1:94929340-94929490	K562	blood:	n/a	n/a
40	CTCF	chr1:94929380-94929530	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr1:94929380-94929530	HAc	cerebellar:	n/a	n/a
42	CTCF	chr1:94929200-94929586	A549	lung:	n/a	n/a
43	CTCF	chr1:94929380-94929530	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr1:94929333-94929584	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr1:94929960-94930110	HMEC	breast:	n/a	n/a
46	CTCF	chr1:94929360-94929510	GM12878	blood:	n/a	n/a
47	CTCF	chr1:94929360-94929510	GM12873	blood:	n/a	n/a
48	CTCF	chr1:94929400-94929550	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:94929380-94929530	HVMF	connective:	n/a	n/a
50	CTCF	chr1:94929400-94929550	AG04449	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94929484-94929534	HRCEpiC	kidney:	n/a
2	chr1:94929484-94929534	GM12891	blood:	n/a
3	chr1:94929484-94929534	ECC-1	luminal epithelium:	n/a
4	chr1:94929484-94929534	MCF-7	breast:	n/a
5	chr1:94929484-94929534	BJ	skin:	n/a
6	chr1:94929484-94929534	HIPEpiC	eye:	n/a
7	chr1:94929484-94929534	RPTEC	kidney:	n/a
8	chr1:94929484-94929534	HRE	kidney:	n/a
9	chr1:94929484-94929534	SK-N-MC	brain:	n/a
10	chr1:94929484-94929534	SAEC	small airway:	n/a
11	chr1:94929484-94929534	GM19239	blood:	n/a
12	chr1:94929484-94929534	ProgFib	skin:	n/a
13	chr1:94929484-94929534	HUVEC	blood vessel:	n/a
14	chr1:94929484-94929534	HNPCEpiC	eye:	n/a
15	chr1:94929484-94929534	Caco-2	colon:	n/a
16	chr1:94929484-94929534	Hepatocyte	liver:	n/a
17	chr1:94929484-94929534	PANC-1	pancreas:	n/a
18	chr1:94929484-94929534	U87	brain:	n/a
19	chr1:94929484-94929534	AoSMC	blood vessel:	n/a
20	chr1:94929484-94929534	BE2_C	brain:	n/a
21	chr1:94929484-94929534	LNCaP	prostate:	n/a
22	chr1:94929484-94929534	NHDF-neo	bronchial:	n/a
23	chr1:94929484-94929534	AG10803	skin:	n/a
24	chr1:94929484-94929534	HRPEpiC	eye:	n/a
25	chr1:94929484-94929534	T-47D	breast:	n/a
26	chr1:94929484-94929534	AG04449	skin:	fetal
27	chr1:94929484-94929534	PrEC	prostate:	n/a
28	chr1:94929484-94929534	CMK	blood:	n/a
29	chr1:94929484-94929534	HCM	heart:	n/a
30	chr1:94929484-94929534	GM12892	blood:	n/a
31	chr1:94929484-94929534	ovcar-3	ovarian:	n/a
32	chr1:94929484-94929534	SK-N-SH	brain:	n/a
33	chr1:94929484-94929534	IMR90	lung:	fetal
34	chr1:94929484-94929534	NH-A	brain:	n/a
35	chr1:94929484-94929534	NB4	blood:	n/a
36	chr1:94929484-94929534	HCF	heart:	n/a
37	chr1:94929484-94929534	HCPEpiC	choroid plexus:	n/a
38	chr1:94929484-94929534	AG09319	gingival:	n/a
39	chr1:94929484-94929534	Jurkat	blood:	n/a
40	chr1:94929484-94929534	HAEpiC	amniotic membrane:	n/a
41	chr1:94929484-94929534	HEEpiC	esophagus:	n/a
42	chr1:94929484-94929534	AG04450	lung:	fetal
43	chr1:94929484-94929534	A549	lung:	n/a
44	chr1:94929484-94929534	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:94929484-94929534	PFSK-1	brain:	n/a
46	chr1:94929484-94929534	HepG2	liver:	n/a
47	chr1:94929484-94929534	H1-hESC	embryonic stem cell:	embryo
48	chr1:94929484-94929534	K562	blood:	n/a
49	chr1:94929484-94929534	Hela-S3	cervix:	n/a
50	chr1:94929484-94929534	HMEC	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94816155..94817816-chr1:94928944..94931018,2	MCF-7	breast:
2	chr1:94883223..94885583-chr1:94928116..94929855,2	MCF-7	breast:
3	chr1:94923038..94925155-chr1:94932732..94934568,2	K562	blood:
4	chr1:94510948..94511922-chr1:94929239..94929819,2	K562	blood:
5	chr1:94923038..94925155-chr1:94932732..94934568,2	K562	blood:
6	chr1:94883768..94885488-chr1:94926929..94929559,2	MCF-7	breast:
7	chr1:94941332..94943153-chr1:94956990..94959761,2	MCF-7	breast:
8	chr1:94526680..94527603-chr1:94928967..94929584,2	K562	blood:
9	chr1:94901652..94904489-chr1:94917080..94919308,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-3	chr1:94917576-94917751	l_89_chr1:94917575-94970548_76bGuttman_hLF

No data

Variant related genes	Relation type
ABCD3	TF binding region
ABCD3	CpG island
ENSG00000117528	chromatin interactions
ENSG00000198691	chromatin interactions

Extended variants
information (count: 901 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs598962	chr1:94916649-94916650	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113083170	chr1:94916728-94916729	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550659115	chr1:94916754-94916755	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183367552	chr1:94916769-94916770	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543405663	chr1:94916790-94916791	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187266132	chr1:94916835-94916836	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573498814	chr1:94916836-94916837	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536121069	chr1:94916858-94916859	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563676988	chr1:94916933-94916934	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77746791	chr1:94916985-94916986	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574464549	chr1:94917001-94917002	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543451701	chr1:94917002-94917003	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191897867	chr1:94917011-94917012	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576832326	chr1:94917058-94917059	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376501273	chr1:94917078-94917079	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559094966	chr1:94917079-94917080	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570555236	chr1:94917094-94917095	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528289466	chr1:94917158-94917159	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541708037	chr1:94917171-94917172	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138980020	chr1:94917339-94917340	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs578150166	chr1:94917385-94917386	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4148057	chr1:94917402-94917403	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs563361968	chr1:94917432-94917433	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531941706	chr1:94917479-94917480	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560889699	chr1:94917499-94917500	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570758423	chr1:94917550-94917551	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373751316	chr1:94917598-94917599	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs72727492	chr1:94917600-94917601	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182773825	chr1:94917611-94917612	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs77461205	chr1:94917633-94917634	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs536084499	chr1:94917639-94917640	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs556092333	chr1:94917663-94917664	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs370661377	chr1:94917683-94917684	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs374562189	chr1:94917687-94917688	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs78294493	chr1:94917729-94917730	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs188443579	chr1:94917738-94917739	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs543051909	chr1:94917788-94917789	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374567691	chr1:94917795-94917796	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556870994	chr1:94917799-94917800	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576788396	chr1:94917815-94917816	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562935011	chr1:94917874-94917875	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192272247	chr1:94918015-94918016	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552687773	chr1:94918019-94918020	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183917242	chr1:94918098-94918099	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112177576	chr1:94918109-94918110	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368540646	chr1:94918120-94918121	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371811693	chr1:94918124-94918125	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530568682	chr1:94918132-94918133	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541660077	chr1:94918141-94918142	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187806146	chr1:94918156-94918157	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD

Chromatin state (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94908600-94918800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:94910600-94928600	Weak transcription	A549	lung
3	chr1:94913800-94974200	Weak transcription	Psoas Muscle	Psoas
4	chr1:94914200-94917600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:94914200-94917800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr1:94914200-94917800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
7	chr1:94914200-94917800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
8	chr1:94914200-94918000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
9	chr1:94914200-94918000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
10	chr1:94914200-94918800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:94914200-94951800	Weak transcription	Brain Angular Gyrus	brain
12	chr1:94914400-94917600	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
13	chr1:94914400-94918000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr1:94914400-94918000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr1:94914400-94918000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
16	chr1:94914400-94918200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
17	chr1:94914400-94918200	ZNF genes & repeats	Primary T cells from cord blood	blood
18	chr1:94914400-94918800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:94914400-94918800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
20	chr1:94914400-94918800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr1:94914600-94916800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:94914600-94916800	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
23	chr1:94914600-94917400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:94914600-94917600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
25	chr1:94914600-94918000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:94914600-94918000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
27	chr1:94914600-94918000	ZNF genes & repeats	Dnd41	blood
28	chr1:94914600-94918800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr1:94914600-94918800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
30	chr1:94914600-94918800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
31	chr1:94914600-94920000	ZNF genes & repeats	Fetal Intestine Large	intestine
32	chr1:94914800-94916800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:94914800-94916800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
34	chr1:94914800-94917600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr1:94914800-94917600	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
36	chr1:94914800-94917800	ZNF genes & repeats	Primary B cells from cord blood	blood
37	chr1:94914800-94918000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:94914800-94985800	Weak transcription	NHLF	lung
39	chr1:94915400-94929800	Weak transcription	Hela-S3	cervix
40	chr1:94915400-94930400	Weak transcription	Brain Anterior Caudate	brain
41	chr1:94915400-94934000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:94915400-94993200	Weak transcription	HSMMtube	muscle
43	chr1:94915800-94917200	Strong transcription	Liver	Liver
44	chr1:94915800-94918200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:94915800-94924600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:94915800-94925400	Weak transcription	Fetal Kidney	kidney
47	chr1:94915800-94925400	Weak transcription	HMEC	breast
48	chr1:94915800-94929400	Weak transcription	Stomach Smooth Muscle	stomach
49	chr1:94915800-94930600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr1:94915800-94935000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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