Variant report

Variant	nsv1006022
Chromosome Location	chr1:91768640-91831196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:143)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:143 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:91827797-91827927	K562	blood:	n/a	n/a
2	ATF1	chr1:91774210-91774371	K562	blood:	n/a	n/a
3	BHLHE40	chr1:91774276-91774286	K562	blood:	n/a	n/a
4	CBX3	chr1:91773310-91773738	HCT-116	colon:	n/a	n/a
5	CBX3	chr1:91773385-91773739	HCT-116	colon:	n/a	n/a
6	CBX3	chr1:91773307-91773736	K562	blood:	n/a	n/a
7	CBX3	chr1:91819676-91819873	K562	blood:	n/a	n/a
8	CBX3	chr1:91773349-91773654	K562	blood:	n/a	n/a
9	CCNT2	chr1:91774161-91774454	K562	blood:	n/a	n/a
10	CEBPB	chr1:91815072-91815443	K562	blood:	n/a	chr1:91815251-91815262
11	CEBPB	chr1:91768637-91768689	HepG2	liver:	n/a	chr1:91768644-91768655
12	CEBPB	chr1:91815163-91815367	K562	blood:	n/a	chr1:91815251-91815262
13	CEBPB	chr1:91768629-91768698	K562	blood:	n/a	chr1:91768644-91768655
14	CEBPB	chr1:91815145-91815427	IMR90	lung:	n/a	chr1:91815251-91815262
15	CEBPB	chr1:91815120-91815377	HepG2	liver:	n/a	chr1:91815251-91815262
16	CEBPB	chr1:91815106-91815377	H1-hESC	embryonic stem cell:	n/a	chr1:91815251-91815262
17	CEBPB	chr1:91815091-91815433	Hela-S3	cervix:	n/a	chr1:91815251-91815262
18	CEBPB	chr1:91768577-91768801	IMR90	lung:	n/a	chr1:91768644-91768655
19	CEBPB	chr1:91815072-91815430	K562	blood:	n/a	chr1:91815251-91815262
20	CEBPD	chr1:91774127-91774523	K562	blood:	n/a	n/a
21	CEBPD	chr1:91774037-91774495	K562	blood:	n/a	n/a
22	CTCF	chr1:91804015-91804098	K562	blood:	n/a	n/a
23	CTCF	chr1:91804020-91804170	GM12872	blood:	n/a	n/a
24	CTCF	chr1:91804000-91804150	GM12872	blood:	n/a	n/a
25	CTCF	chr1:91804040-91804190	GM12878	blood:	n/a	n/a
26	CTCF	chr1:91796654-91796720	GM13976	blood:	n/a	n/a
27	CTCF	chr1:91804002-91804129	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:91795401-91795471	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr1:91803880-91804030	GM12878	blood:	n/a	n/a
30	CTCF	chr1:91803900-91804050	K562	blood:	n/a	n/a
31	CTCF	chr1:91807053-91807090	GM13976	blood:	n/a	n/a
32	EP300	chr1:91815091-91815448	K562	blood:	n/a	n/a
33	EP300	chr1:91774124-91774509	K562	blood:	n/a	n/a
34	FOS	chr1:91801266-91801445	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:91801334-91801378	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:91780201-91780503	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:91780284-91780484	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:91801298-91801448	MCF10A-Er-Src	breast:	n/a	n/a
39	GABPA	chr1:91815094-91815369	K562	blood:	n/a	n/a
40	GATA1	chr1:91774025-91774708	K562	blood:	n/a	n/a
41	GATA1	chr1:91774083-91774471	PBDE	blood:	n/a	n/a
42	GATA2	chr1:91774045-91774502	K562	blood:	n/a	n/a
43	GATA2	chr1:91824489-91824827	SH-SY5Y	brain:	n/a	n/a
44	GATA2	chr1:91809570-91809792	K562	blood:	n/a	n/a
45	GATA2	chr1:91815056-91815420	K562	blood:	n/a	n/a
46	GATA2	chr1:91774118-91774419	K562	blood:	n/a	n/a
47	GATA3	chr1:91775471-91775671	SH-SY5Y	brain:	n/a	n/a
48	HMGN3	chr1:91774167-91774380	K562	blood:	n/a	n/a
49	HNF4A	chr1:91812520-91812667	HepG2	liver:	n/a	n/a
50	IRF1	chr1:91774250-91774450	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:91814033-91814083	AG04449	skin:	fetal
2	chr1:91814033-91814083	MCF10A-Er-Src	breast:	n/a
3	chr1:91814033-91814083	AG09309	skin:	n/a
4	chr1:91814033-91814083	GM06990	blood:	n/a
5	chr1:91814033-91814083	GM19239	blood:	n/a
6	chr1:91814033-91814083	HCF	heart:	n/a
7	chr1:91814033-91814083	HEK293	kidney:	embryo
8	chr1:91814033-91814083	PFSK-1	brain:	n/a
9	chr1:91814033-91814083	SK-N-SH_RA	brain:	n/a
10	chr1:91814033-91814083	SK-N-SH	brain:	n/a
11	chr1:91814033-91814083	HMEC	breast:	n/a
12	chr1:91814033-91814083	NH-A	brain:	n/a
13	chr1:91814033-91814083	NHDF-neo	bronchial:	n/a
14	chr1:91814033-91814083	HAEpiC	amniotic membrane:	n/a
15	chr1:91814033-91814083	A549	lung:	n/a
16	chr1:91814033-91814083	CMK	blood:	n/a
17	chr1:91814033-91814083	Caco-2	colon:	n/a
18	chr1:91814033-91814083	HRE	kidney:	n/a
19	chr1:91814033-91814083	AoSMC	blood vessel:	n/a
20	chr1:91814033-91814083	HepG2	liver:	n/a
21	chr1:91814033-91814083	H1-hESC	embryonic stem cell:	embryo
22	chr1:91814033-91814083	HEEpiC	esophagus:	n/a
23	chr1:91814033-91814083	RPTEC	kidney:	n/a
24	chr1:91814033-91814083	BE2_C	brain:	n/a
25	chr1:91814033-91814083	HCPEpiC	choroid plexus:	n/a
26	chr1:91814033-91814083	MCF-7	breast:	n/a
27	chr1:91814033-91814083	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:91814033-91814083	HL-60	blood:	n/a
29	chr1:91814033-91814083	LNCaP	prostate:	n/a
30	chr1:91814033-91814083	ECC-1	luminal epithelium:	n/a
31	chr1:91814033-91814083	HCM	heart:	n/a
32	chr1:91814033-91814083	SAEC	small airway:	n/a
33	chr1:91814033-91814083	GM12891	blood:	n/a
34	chr1:91814033-91814083	U87	brain:	n/a
35	chr1:91814033-91814083	NB4	blood:	n/a
36	chr1:91814033-91814083	Hela-S3	cervix:	n/a
37	chr1:91814033-91814083	ProgFib	skin:	n/a
38	chr1:91814033-91814083	K562	blood:	n/a
39	chr1:91814033-91814083	PrEC	prostate:	n/a
40	chr1:91814033-91814083	AG09319	gingival:	n/a
41	chr1:91814033-91814083	HCT-116	colon:	n/a
42	chr1:91814033-91814083	HUVEC	blood vessel:	n/a
43	chr1:91814033-91814083	GM12892	blood:	n/a
44	chr1:91814033-91814083	AG04450	lung:	fetal
45	chr1:91814033-91814083	HRCEpiC	kidney:	n/a
46	chr1:91814033-91814083	HRPEpiC	eye:	n/a
47	chr1:91814033-91814083	NT2-D1	testis:	n/a
48	chr1:91814033-91814083	HIPEpiC	eye:	n/a
49	chr1:91814033-91814083	Jurkat	blood:	n/a
50	chr1:91814033-91814083	AG10803	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:91815411..91816307-chr17:57922310..57923133,2	MCF-7	breast:
2	chr1:91786405..91788910-chr1:91799387..91801097,2	K562	blood:
3	chr1:91790980..91792779-chr1:91870013..91871774,2	K562	blood:
4	chr1:91786405..91788910-chr1:91799387..91801097,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HFM1-2	chr1:91784850-91784947	NONHSAT004431
2	lnc-HFM1-2	chr1:91781697-91781741	NONHSAT004431
3	lnc-HFM1-2	chr1:91794395-91794494	NONHSAT004431
4	lnc-HFM1-2	chr1:91788507-91788554	NONHSAT004431
5	lnc-HFM1-2	chr1:91790232-91790323	NONHSAT004431

No data

Variant related genes	Relation type
HFM1	TF binding region
FEN1P1	TF binding region
HFM1	CpG island
FEN1P1	CpG island
ENSG00000162669	chromatin interactions

Extended variants
information (count: 2181 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2181 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56355433	chr1:91768681-91768682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188168615	chr1:91768711-91768712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117071921	chr1:91768730-91768731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575351360	chr1:91768752-91768753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75860040	chr1:91768755-91768756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539422127	chr1:91768786-91768787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367776088	chr1:91768818-91768819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572909162	chr1:91768841-91768842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34600283	chr1:91768870-91768871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs561571757	chr1:91768894-91768895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573483808	chr1:91768938-91768939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116833009	chr1:91768940-91768941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562435904	chr1:91768982-91768983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192822687	chr1:91769001-91769002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184372411	chr1:91769010-91769011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56796555	chr1:91769035-91769036	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181959828	chr1:91769055-91769056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115184821	chr1:91769095-91769096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376295091	chr1:91769197-91769198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs36114555	chr1:91769227-91769228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184809823	chr1:91769233-91769234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568705737	chr1:91769287-91769288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190582288	chr1:91769349-91769350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551342963	chr1:91769381-91769382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569543450	chr1:91769433-91769434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs417762	chr1:91769471-91769472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557755816	chr1:91769489-91769490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572726768	chr1:91769492-91769493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533919486	chr1:91769556-91769557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533633450	chr1:91769563-91769564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555032010	chr1:91769568-91769569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573543441	chr1:91769629-91769630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544007925	chr1:91769632-91769633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540938719	chr1:91769656-91769657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577887048	chr1:91769658-91769659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544948309	chr1:91769673-91769674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199536724	chr1:91769678-91769679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117694028	chr1:91769707-91769708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528461295	chr1:91769712-91769713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181041511	chr1:91769833-91769834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143738474	chr1:91769923-91769924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34182924	chr1:91770005-91770006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs397861133	chr1:91770007-91770008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529366592	chr1:91770054-91770055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113944393	chr1:91770164-91770165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12746156	chr1:91770170-91770171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs533706428	chr1:91770182-91770183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551769310	chr1:91770184-91770185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566501180	chr1:91770185-91770186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58215219	chr1:91770191-91770192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:91749000-91774600	Weak transcription	Ovary	ovary
2	chr1:91772800-91793800	Weak transcription	Left Ventricle	heart
3	chr1:91773600-91796200	Weak transcription	Fetal Kidney	kidney
4	chr1:91774200-91774800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr1:91774200-91775000	ZNF genes & repeats	Fetal Lung	lung
6	chr1:91774200-91777200	Weak transcription	Fetal Brain Female	brain
7	chr1:91774600-91774800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:91774600-91774800	ZNF genes & repeats	Ovary	ovary
9	chr1:91774600-91775400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:91774600-91776200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:91774600-91777600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr1:91774600-91778800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr1:91774800-91777200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:91774800-91777400	Weak transcription	Ovary	ovary
15	chr1:91774800-91794400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr1:91775000-91777200	Weak transcription	Fetal Lung	lung
17	chr1:91775000-91793800	Weak transcription	Pancreas	Pancrea
18	chr1:91775200-91777200	Weak transcription	Brain Germinal Matrix	brain
19	chr1:91775200-91777200	Weak transcription	Fetal Stomach	stomach
20	chr1:91775200-91794000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr1:91775400-91776600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:91775800-91777600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:91776200-91776600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:91776600-91777200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr1:91776600-91793800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:91776800-91777400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr1:91776800-91777800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:91777000-91780400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:91777200-91777600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr1:91777200-91777600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
31	chr1:91777200-91777600	ZNF genes & repeats	Fetal Brain Female	brain
32	chr1:91777200-91777800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:91777200-91778000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:91777200-91778000	Strong transcription	Brain Germinal Matrix	brain
35	chr1:91777200-91778000	Strong transcription	Fetal Lung	lung
36	chr1:91777200-91778200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:91777200-91778600	Strong transcription	Fetal Stomach	stomach
38	chr1:91777400-91777600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
39	chr1:91777400-91778000	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr1:91777400-91778600	Strong transcription	Ovary	ovary
41	chr1:91777600-91777800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:91777600-91778000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr1:91777600-91778000	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr1:91777600-91781400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:91777600-91790600	Weak transcription	Fetal Brain Female	brain
46	chr1:91777600-91790600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr1:91777600-91790800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr1:91777600-91794000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr1:91777800-91778000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:91777800-91778000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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