Variant report

Variant	nsv540046
Chromosome Location	chr9:11952521-12357074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:715)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12328968-12329168	HepG2	liver:	n/a	n/a
2	BACH1	chr9:12170667-12170713	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:12292536-12292567	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr9:12230772-12231081	GM12878	blood:	n/a	n/a
5	BATF	chr9:12329455-12329670	GM12878	blood:	n/a	n/a
6	BCLAF1	chr9:12329426-12329668	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:12329021-12329257	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:12328995-12329158	K562	blood:	n/a	n/a
9	BHLHE40	chr9:12328884-12329725	HepG2	liver:	n/a	n/a
10	BRCA1	chr9:12011400-12011402	GM12878	blood:	n/a	n/a
11	CBX3	chr9:12054451-12054644	K562	blood:	n/a	n/a
12	CEBPB	chr9:11968269-11968582	A549	lung:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
13	CEBPB	chr9:11968320-11968531	HepG2	liver:	n/a	chr9:11968445-11968456 chr9:11968447-11968456 chr9:11968446-11968457 chr9:11968445-11968458
14	CEBPB	chr9:12193945-12194181	A549	lung:	n/a	chr9:12194071-12194082 chr9:12194071-12194084
15	CEBPB	chr9:12119993-12120079	A549	lung:	n/a	chr9:12120059-12120068 chr9:12120057-12120070 chr9:12120057-12120068
16	CEBPB	chr9:12195471-12195788	IMR90	lung:	n/a	chr9:12195611-12195622
17	CEBPB	chr9:12288039-12288167	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:11959593-11959818	IMR90	lung:	n/a	chr9:11959657-11959668
19	CEBPB	chr9:12012267-12012412	A549	lung:	n/a	n/a
20	CEBPB	chr9:11959508-11959839	HepG2	liver:	n/a	chr9:11959657-11959668
21	CEBPB	chr9:12208833-12209071	HepG2	liver:	n/a	chr9:12208898-12208909 chr9:12208899-12208908 chr9:12208897-12208910
22	CEBPB	chr9:12195456-12195797	HepG2	liver:	n/a	chr9:12195611-12195622
23	CEBPB	chr9:12129071-12129335	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:12180768-12180970	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:12195470-12195708	H1-hESC	embryonic stem cell:	n/a	chr9:12195611-12195622
26	CEBPB	chr9:12195488-12195695	K562	blood:	n/a	chr9:12195611-12195622
27	CEBPB	chr9:11959566-11959766	K562	blood:	n/a	chr9:11959657-11959668
28	CHD1	chr9:12314638-12314797	GM12878	blood:	n/a	n/a
29	CHD2	chr9:12319226-12319370	GM12878	blood:	n/a	n/a
30	CHD2	chr9:12314733-12314838	GM12878	blood:	n/a	n/a
31	CTCF	chr9:12195560-12195710	HEK293	kidney:	n/a	n/a
32	CTCF	chr9:12329390-12329697	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr9:12329520-12329670	A549	lung:	n/a	n/a
34	CTCF	chr9:12195600-12195750	NHEK	skin:	n/a	n/a
35	CTCF	chr9:12329466-12329689	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr9:12329500-12329650	GM12875	blood:	n/a	n/a
37	CTCF	chr9:12329447-12329704	GM10248	blood:	n/a	n/a
38	CTCF	chr9:12053853-12053871	GM20000	blood:	n/a	n/a
39	CTCF	chr9:12329425-12329629	T-47D	breast:	n/a	n/a
40	CTCF	chr9:12329500-12329650	K562	blood:	n/a	n/a
41	CTCF	chr9:12329520-12329670	GM12870	blood:	n/a	n/a
42	CTCF	chr9:12329480-12329630	NB4	blood:	n/a	n/a
43	CTCF	chr9:12224065-12224152	GM13976	blood:	n/a	n/a
44	CTCF	chr9:12092280-12092430	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr9:12328920-12329070	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr9:12329384-12329765	IMR90	lung:	n/a	n/a
47	CTCF	chr9:12329367-12329706	K562	blood:	n/a	n/a
48	CTCF	chr9:12329520-12329670	BJ	skin:	n/a	n/a
49	CTCF	chr9:12329500-12329650	GM12871	blood:	n/a	n/a
50	CTCF	chr9:12329500-12329650	HMF	breast:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
2	chr18:21570976..21573123-chr9:12145530..12147030,2	MCF-7	breast:
3	chr9:10855828..10856443-chr9:12329128..12329639,2	MCF-7	breast:
4	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
5	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:
6	chr9:10365979..10366914-chr9:12329143..12329893,2	MCF-7	breast:
7	chr9:12094328..12096426-chr9:12096756..12098736,2	K562	blood:
8	chr9:12268631..12271178-chr9:12273434..12276211,2	K562	blood:
9	chr16:89002000..89004763-chr9:12244429..12246932,2	MCF-7	breast:
10	chr9:12182493..12185046-chr9:12186407..12189303,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
2	lnc-MPDZ-2	chr9:12139007-12139044	XLOC_007648
3	lnc-MPDZ-2	chr9:12146273-12146401	XLOC_007648
4	lnc-MPDZ-2	chr9:12098660-12099015	XLOC_007648
5	lnc-MPDZ-2	chr9:12159117-12159147	XLOC_007648
6	lnc-MPDZ-9	chr9:12088660-12089015	NONHSAT130219
7	lnc-TYRP1-4	chr9:12287320-12288238	NONHSAT130222
8	lnc-MPDZ-9	chr9:12106821-12106865	NONHSAT130219
9	lnc-MPDZ-9	chr9:12149117-12149147	NONHSAT130219
10	lnc-MPDZ-9	chr9:12136273-12136401	NONHSAT130219
11	lnc-MPDZ-2	chr9:12116821-12116865	XLOC_007648
12	lnc-MPDZ-2	chr9:12098714-12099015	XLOC_007648

No data

Variant related genes	Relation type
ENSG00000231491	TF binding region
ENSG00000224935	TF binding region
RNU2-47P	TF binding region
ENSG00000168234	chromatin interactions
ENSG00000261226	chromatin interactions

Extended variants
information (count: 5679 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:5679 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561726534	chr9:11966629-11966630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376107697	chr9:11966655-11966656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534257196	chr9:11966657-11966658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552296750	chr9:11966683-11966684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577140392	chr9:11966742-11966743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527340733	chr9:11966759-11966760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79778413	chr9:11966764-11966765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558457957	chr9:11966778-11966779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113669988	chr9:11966809-11966810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369437097	chr9:11966822-11966823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544049518	chr9:11966823-11966824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191746685	chr9:11966851-11966852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs55643469	chr9:11966916-11966917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368300087	chr9:11966917-11966918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184774663	chr9:11966920-11966921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559917490	chr9:11966930-11966931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs60730497	chr9:11966944-11966945	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551873554	chr9:11966964-11966965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569614308	chr9:11966965-11966966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531993965	chr9:11966990-11966991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35747547	chr9:11966996-11966997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4490942	chr9:11967011-11967012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189997023	chr9:11967012-11967013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10960402	chr9:11967033-11967034	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552773524	chr9:11967035-11967036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570841597	chr9:11967036-11967037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181811436	chr9:11967051-11967052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141706880	chr9:11967066-11967067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565925653	chr9:11967088-11967089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10960403	chr9:11967114-11967115	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544061700	chr9:11967135-11967136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554361686	chr9:11967150-11967151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73646829	chr9:11967151-11967152	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs540034887	chr9:11967190-11967191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150108182	chr9:11967214-11967215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576859275	chr9:11967234-11967235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185745254	chr9:11967235-11967236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531695765	chr9:11967292-11967293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556661586	chr9:11967300-11967301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532059148	chr9:11967349-11967350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548870670	chr9:11967357-11967358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138543596	chr9:11967379-11967380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73646831	chr9:11968801-11968802	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs190821281	chr9:11968812-11968813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539206358	chr9:11968816-11968817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569770218	chr9:11968834-11968835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10960404	chr9:11968855-11968856	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs555358736	chr9:11968912-11968913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370239073	chr9:11968961-11968962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571919768	chr9:11968983-11968984	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Type 2 diabetes	21526130	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:11966600-11967200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:11966800-11967200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:11966800-11967200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:11966800-11967400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr9:11968800-11969000	Enhancers	Pancreas	Pancrea
6	chr9:11972800-11973200	Enhancers	Placenta Amnion	Placenta Amnion
7	chr9:11975000-11975200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr9:11975600-11976200	Enhancers	Fetal Brain Male	brain
9	chr9:11976000-11976200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr9:11977400-11977600	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr9:11991400-11994000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr9:11991800-11992200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:11991800-11992200	Enhancers	Fetal Heart	heart
14	chr9:11991800-11993400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:11992400-11993200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr9:11993000-11993800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr9:11995800-11996600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:11995800-11998200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:11996600-11996800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:12017400-12019600	Weak transcription	Fetal Heart	heart
21	chr9:12019600-12021400	Enhancers	Fetal Heart	heart
22	chr9:12046400-12046800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr9:12046800-12048000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr9:12048000-12048400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr9:12054200-12054600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:12057600-12059000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr9:12058400-12060400	Enhancers	Fetal Intestine Large	intestine
28	chr9:12059000-12060000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:12060000-12065800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:12060200-12060400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr9:12060400-12061400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr9:12060400-12065000	Weak transcription	Fetal Intestine Large	intestine
33	chr9:12061400-12061800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr9:12061400-12062000	Enhancers	Placenta Amnion	Placenta Amnion
35	chr9:12061600-12061800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr9:12061800-12064200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr9:12064200-12065600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr9:12065000-12065800	Enhancers	Fetal Intestine Large	intestine
39	chr9:12076400-12076600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
40	chr9:12076400-12076800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:12076600-12076800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
42	chr9:12091200-12096400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr9:12091600-12092600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr9:12091800-12092200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr9:12092600-12096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:12096200-12096400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:12096400-12101600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:12101600-12102200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr9:12101600-12102400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:12101800-12102800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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