Variant report

Variant	nsv873065
Chromosome Location	chr1:197027749-197076194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:197036264-197036959	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:197035700-197036063	HepG2	liver:	n/a	n/a
3	ATF1	chr1:197035585-197035625	K562	blood:	n/a	n/a
4	BACH1	chr1:197072339-197072887	K562	blood:	n/a	n/a
5	BACH1	chr1:197073109-197073136	K562	blood:	n/a	n/a
6	BATF	chr1:197061784-197062055	GM12878	blood:	n/a	n/a
7	BATF	chr1:197065302-197065518	GM12878	blood:	n/a	chr1:197065444-197065455
8	BRCA1	chr1:197067276-197067321	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr1:197049455-197049863	K562	blood:	n/a	n/a
10	CBX3	chr1:197050179-197050900	K562	blood:	n/a	n/a
11	CBX3	chr1:197050255-197050857	K562	blood:	n/a	n/a
12	CEBPB	chr1:197062629-197063024	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:197062648-197063000	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:197059128-197059372	HepG2	liver:	n/a	chr1:197059287-197059298
15	CEBPB	chr1:197062726-197062961	K562	blood:	n/a	n/a
16	CEBPB	chr1:197062650-197062984	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:197062475-197062999	A549	lung:	n/a	n/a
18	CEBPB	chr1:197062761-197062934	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:197035675-197035694	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:197070552-197070638	K562	blood:	n/a	n/a
21	CEBPB	chr1:197036597-197036965	HepG2	liver:	n/a	chr1:197036772-197036783
22	CEBPB	chr1:197035462-197035745	HepG2	liver:	n/a	chr1:197035618-197035629 chr1:197035617-197035630 chr1:197035617-197035628
23	CEBPB	chr1:197075977-197076481	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr1:197076040-197076417	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr1:197036638-197036866	HepG2	liver:	n/a	chr1:197036772-197036783
26	CHD2	chr1:197071837-197071866	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:197072563-197073085	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr1:197072318-197072793	K562	blood:	n/a	n/a
29	CHD2	chr1:197070949-197071464	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr1:197070875-197071307	K562	blood:	n/a	n/a
31	CTCF	chr1:197036000-197036150	NHDF-neo	bronchial:	n/a	chr1:197036046-197036062
32	CTCF	chr1:197036000-197036150	AoAF	blood vessel:	n/a	chr1:197036046-197036062
33	CTCF	chr1:197032440-197032590	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr1:197032540-197032690	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr1:197035960-197036110	HCPEpiC	choroid plexus:	n/a	chr1:197036046-197036062
36	CTCF	chr1:197035951-197036151	H1-hESC	embryonic stem cell:	n/a	chr1:197036046-197036062
37	CTCF	chr1:197035917-197036131	A549	lung:	n/a	chr1:197036046-197036062
38	CTCF	chr1:197032440-197032590	HCFaa	heart:	n/a	n/a
39	CTCF	chr1:197032440-197032590	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr1:197032480-197032630	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr1:197040885-197040979	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr1:197035885-197036206	GM12878	blood:	n/a	chr1:197036046-197036062
43	CTCF	chr1:197036000-197036150	HepG2	liver:	n/a	chr1:197036046-197036062
44	CTCF	chr1:197032480-197032630	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:197044915-197044971	GM20000	blood:	n/a	n/a
46	CTCF	chr1:197035880-197036030	RPTEC	kidney:	n/a	n/a
47	CTCF	chr1:197032440-197032590	GM12866	blood:	n/a	n/a
48	CTCF	chr1:197032380-197032530	K562	blood:	n/a	n/a
49	CTCF	chr1:197032420-197032570	BE2_C	brain:	n/a	n/a
50	CTCF	chr1:197035980-197036130	AG10803	skin:	n/a	chr1:197036046-197036062

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:197030122-197030172	Hepatocyte	liver:	n/a
2	chr1:197037504-197037554	Caco-2	colon:	n/a
3	chr1:197030122-197030172	HCT-116	colon:	n/a
4	chr1:197037504-197037554	SK-N-MC	brain:	n/a
5	chr1:197037504-197037554	HMEC	breast:	n/a
6	chr1:197030122-197030172	HRPEpiC	eye:	n/a
7	chr1:197037732-197037782	HCT-116	colon:	n/a
8	chr1:197037504-197037554	SK-N-SH	brain:	n/a
9	chr1:197037732-197037782	Caco-2	colon:	n/a
10	chr1:197037504-197037554	HRE	kidney:	n/a
11	chr1:197037732-197037782	HEEpiC	esophagus:	n/a
12	chr1:197037732-197037782	H1-hESC	embryonic stem cell:	embryo
13	chr1:197030122-197030172	HCF	heart:	n/a
14	chr1:197030122-197030172	NB4	blood:	n/a
15	chr1:197037732-197037782	Hela-S3	cervix:	n/a
16	chr1:197030122-197030172	RPTEC	kidney:	n/a
17	chr1:197037732-197037782	NH-A	brain:	n/a
18	chr1:197030122-197030172	HRCEpiC	kidney:	n/a
19	chr1:197037732-197037782	LNCaP	prostate:	n/a
20	chr1:197030122-197030172	T-47D	breast:	n/a
21	chr1:197037504-197037554	HCPEpiC	choroid plexus:	n/a
22	chr1:197037732-197037782	HEK293	kidney:	embryo
23	chr1:197037732-197037782	HepG2	liver:	n/a
24	chr1:197030122-197030172	ECC-1	luminal epithelium:	n/a
25	chr1:197037504-197037554	NB4	blood:	n/a
26	chr1:197037732-197037782	HNPCEpiC	eye:	n/a
27	chr1:197037504-197037554	GM19239	blood:	n/a
28	chr1:197037732-197037782	SK-N-SH	brain:	n/a
29	chr1:197037732-197037782	MCF10A-Er-Src	breast:	n/a
30	chr1:197037504-197037554	NH-A	brain:	n/a
31	chr1:197037504-197037554	AG09309	skin:	n/a
32	chr1:197037732-197037782	BE2_C	brain:	n/a
33	chr1:197030122-197030172	AG10803	skin:	n/a
34	chr1:197037732-197037782	AG04449	skin:	fetal
35	chr1:197037732-197037782	SKMC	muscle:	n/a
36	chr1:197037504-197037554	HRCEpiC	kidney:	n/a
37	chr1:197030122-197030172	AG09319	gingival:	n/a
38	chr1:197037504-197037554	H1-hESC	embryonic stem cell:	embryo
39	chr1:197037504-197037554	HL-60	blood:	n/a
40	chr1:197037504-197037554	PrEC	prostate:	n/a
41	chr1:197037732-197037782	AG10803	skin:	n/a
42	chr1:197037504-197037554	ECC-1	luminal epithelium:	n/a
43	chr1:197030122-197030172	MCF10A-Er-Src	breast:	n/a
44	chr1:197037732-197037782	PrEC	prostate:	n/a
45	chr1:197037504-197037554	HEK293	kidney:	embryo
46	chr1:197030122-197030172	AG09309	skin:	n/a
47	chr1:197030122-197030172	HL-60	blood:	n/a
48	chr1:197030122-197030172	Hela-S3	cervix:	n/a
49	chr1:197037732-197037782	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:197037504-197037554	BE2_C	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:197057862..197060422-chr16:85387668..85389752,2	MCF-7	breast:
2	chr1:197055379..197060712-chr1:197061077..197065456,6	K562	blood:
3	chr1:197071674..197075370-chr1:197103633..197105995,3	K562	blood:
4	chr1:197055379..197060712-chr1:197061077..197065456,6	K562	blood:
5	chr1:197063964..197065535-chr1:197110090..197112434,2	K562	blood:
6	chr1:197056210..197058041-chr1:197063459..197065342,2	K562	blood:
7	chr1:197068919..197071341-chr1:197120763..197122532,2	K562	blood:
8	chr1:196988548..196990975-chr1:197072466..197074203,2	K562	blood:
9	chr1:197017524..197019536-chr1:197026374..197028329,2	K562	blood:
10	chr1:197056210..197058041-chr1:197063459..197065342,2	K562	blood:
11	chr1:197055911..197057601-chr1:197071905..197074191,2	K562	blood:
12	chr1:197073799..197075979-chr1:197077836..197079355,2	K562	blood:
13	chr1:196993317..196995109-chr1:197057738..197060458,2	K562	blood:
14	chr1:197055911..197057601-chr1:197071905..197074191,2	K562	blood:
15	chr1:197026462..197029856-chr1:197031681..197034887,3	K562	blood:
16	chr1:197026462..197029856-chr1:197031681..197034887,3	K562	blood:
17	chr1:197075415..197078387-chr1:197103819..197106746,2	K562	blood:
18	chr1:197075217..197076795-chr1:197101256..197102905,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPM-1	chr1:197043802-197043995	l_160_chr1:197043319-197062807_placenta
2	lnc-ASPM-1	chr1:197062778-197062807	l_160_chr1:197043319-197062807_placenta
3	lnc-ASPM-1	chr1:197062778-197062968	NONHSAT008611
4	lnc-ASPM-1	chr1:197043410-197043995	NONHSAT008612
5	lnc-ASPM-1	chr1:197043245-197043995	NONHSAT008611
6	lnc-ASPM-1	chr1:197043320-197043793	l_160_chr1:197043319-197062807_placenta

No data

Variant related genes	Relation type
F13B	TF binding region
F13B	CpG island
ENSG00000066279	chromatin interactions

Extended variants
information (count: 1669 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1669 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17514274	chr1:197027749-197027750	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537426832	chr1:197027768-197027769	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11810678	chr1:197027870-197027871	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571134029	chr1:197027878-197027879	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535251346	chr1:197027884-197027885	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536692054	chr1:197027989-197027990	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188925935	chr1:197028002-197028003	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193233647	chr1:197028010-197028011	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535942529	chr1:197028042-197028043	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557116751	chr1:197028083-197028084	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185362873	chr1:197028130-197028131	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536973499	chr1:197028150-197028151	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17514577	chr1:197028160-197028161	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs17514570	chr1:197028165-197028166	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs540836031	chr1:197028180-197028181	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145582383	chr1:197028324-197028325	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574238572	chr1:197028331-197028332	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577658807	chr1:197028387-197028388	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190268217	chr1:197028413-197028414	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2298883	chr1:197028634-197028635	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs181440711	chr1:197028666-197028667	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564781089	chr1:197028681-197028682	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74987187	chr1:197028686-197028687	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184247670	chr1:197028709-197028710	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574577528	chr1:197028722-197028723	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568662675	chr1:197028767-197028768	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140381752	chr1:197028769-197028770	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551032255	chr1:197028778-197028779	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569225121	chr1:197028786-197028787	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188531510	chr1:197028801-197028802	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557689924	chr1:197028880-197028881	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570417272	chr1:197028902-197028903	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180992612	chr1:197028907-197028908	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552787250	chr1:197028993-197028994	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574557270	chr1:197029006-197029007	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145605995	chr1:197029032-197029033	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557036972	chr1:197029101-197029102	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575211557	chr1:197029154-197029155	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545819682	chr1:197029185-197029186	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564068473	chr1:197029223-197029224	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185995396	chr1:197029224-197029225	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540914353	chr1:197029334-197029335	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1332661	chr1:197029345-197029346	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138809324	chr1:197029357-197029358	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555140730	chr1:197029416-197029417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550859190	chr1:197029495-197029496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192115956	chr1:197029499-197029500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533222920	chr1:197029505-197029506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374521116	chr1:197029530-197029531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139285262	chr1:197029534-197029535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197017400-197029400	Strong transcription	Liver	Liver
2	chr1:197029400-197029800	Weak transcription	Liver	Liver
3	chr1:197029800-197031000	Genic enhancers	Liver	Liver
4	chr1:197031000-197033000	Enhancers	Liver	Liver
5	chr1:197031200-197032200	Enhancers	GM12878-XiMat	blood
6	chr1:197032000-197032200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:197032200-197032400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:197032200-197034000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:197033000-197034400	Flanking Active TSS	Liver	Liver
10	chr1:197034000-197034400	Enhancers	HSMMtube	muscle
11	chr1:197034000-197035200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr1:197034200-197034800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:197034200-197035200	Enhancers	Osteobl	bone
14	chr1:197034200-197035800	Enhancers	Fetal Heart	heart
15	chr1:197034400-197035000	Enhancers	Placenta Amnion	Placenta Amnion
16	chr1:197034400-197036600	Active TSS	Liver	Liver
17	chr1:197034600-197035200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:197035400-197036600	Active TSS	Fetal Intestine Large	intestine
19	chr1:197035600-197038000	Enhancers	HepG2	liver
20	chr1:197036600-197036800	Weak transcription	Fetal Intestine Large	intestine
21	chr1:197036600-197037400	Flanking Active TSS	Liver	Liver
22	chr1:197036800-197037600	Enhancers	Fetal Intestine Large	intestine
23	chr1:197037000-197037800	Enhancers	Duodenum Mucosa	Duodenum
24	chr1:197037000-197038000	Enhancers	Fetal Intestine Small	intestine
25	chr1:197037400-197037800	Enhancers	Liver	Liver
26	chr1:197046000-197046600	Enhancers	GM12878-XiMat	blood
27	chr1:197049000-197050400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:197049200-197050800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:197049800-197051800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr1:197050000-197050400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr1:197050000-197052800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chr1:197050200-197050800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:197050200-197051400	Weak transcription	Fetal Kidney	kidney
34	chr1:197050200-197052200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr1:197050200-197052400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:197050400-197050600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr1:197050400-197050800	ZNF genes & repeats	Gastric	stomach
38	chr1:197050400-197051600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
39	chr1:197050400-197051800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr1:197050400-197052000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:197050400-197052200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:197050400-197052200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:197050400-197052200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
44	chr1:197050400-197052200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:197050400-197052200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr1:197050400-197052200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:197050400-197052200	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr1:197050400-197052400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:197050400-197052400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
50	chr1:197050400-197055200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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