Variant report

Variant	nsv1041197
Chromosome Location	chr11:87185278-87227163
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:112)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:112 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr11:87204621-87204917	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr11:87204640-87204899	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:87204666-87205419	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr11:87212560-87212680	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr11:87218880-87219030	HEEpiC	esophagus:	n/a	n/a
6	CTCF	chr11:87212540-87212690	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr11:87212560-87212710	SAEC	small airway:	n/a	n/a
8	CTCF	chr11:87212560-87212710	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr11:87212580-87212730	HCT-116	colon:	n/a	n/a
10	CTCF	chr11:87212560-87212710	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr11:87212557-87212672	A549	lung:	n/a	n/a
12	CTCF	chr11:87212565-87212656	MCF-7	breast:	n/a	n/a
13	CTCF	chr11:87212600-87212750	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr11:87212520-87212670	HEK293	kidney:	n/a	n/a
15	CTCF	chr11:87212580-87212730	HMEC	breast:	n/a	n/a
16	CTCF	chr11:87190940-87191090	HepG2	liver:	n/a	n/a
17	CTCF	chr11:87212580-87212730	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr11:87212540-87212690	Caco-2	colon:	n/a	n/a
19	CTCF	chr11:87212518-87212688	HepG2	liver:	n/a	n/a
20	CTCF	chr11:87212540-87212690	AG09319	gingival:	n/a	n/a
21	CTCF	chr11:87212550-87212690	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:87212520-87212670	K562	blood:	n/a	n/a
23	CTCF	chr11:87212567-87212705	MCF-7	breast:	n/a	n/a
24	CTCF	chr11:87212585-87212675	NHEK	skin:	n/a	n/a
25	CTCF	chr11:87225320-87225470	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr11:87212575-87212647	GM19238	blood:	n/a	n/a
27	CTCF	chr11:87212500-87212650	HCT-116	colon:	n/a	n/a
28	CTCF	chr11:87212571-87212670	Gliobla	brain:	n/a	n/a
29	CTCF	chr11:87225380-87225530	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr11:87212611-87212691	Medullo	brain:	n/a	n/a
31	CTCF	chr11:87212574-87212663	GM12878	blood:	n/a	n/a
32	CTCF	chr11:87212565-87212659	ProgFib	skin:	n/a	n/a
33	CTCF	chr11:87212558-87212660	HepG2	liver:	n/a	n/a
34	CTCF	chr11:87212544-87212671	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr11:87211437-87211459	GM10248	blood:	n/a	n/a
36	CTCF	chr11:87218879-87219010	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr11:87212528-87212730	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:87225320-87225470	HMEC	breast:	n/a	n/a
39	CTCF	chr11:87190840-87190990	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:87212579-87212654	GM13976	blood:	n/a	n/a
41	CTCF	chr11:87225360-87225510	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr11:87212540-87212690	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr11:87212563-87212722	K562	blood:	n/a	n/a
44	CTCF	chr11:87212600-87212750	NHEK	skin:	n/a	n/a
45	CTCF	chr11:87212553-87212677	MCF-7	breast:	n/a	n/a
46	CTCF	chr11:87218900-87219050	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr11:87212460-87212610	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr11:87212568-87212666	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:87212617-87212651	GM12892	blood:	n/a	n/a
50	CTCF	chr11:87224000-87224150	GM12866	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:87224821-87224871	HCT-116	colon:	n/a
2	chr11:87224821-87224871	RPTEC	kidney:	n/a
3	chr11:87204675-87204725	NHDF-neo	bronchial:	n/a
4	chr11:87224821-87224871	NHBE	bronchial:	n/a
5	chr11:87204675-87204725	HEEpiC	esophagus:	n/a
6	chr11:87204675-87204725	SKMC	muscle:	n/a
7	chr11:87224821-87224871	K562	blood:	n/a
8	chr11:87224821-87224871	ProgFib	skin:	n/a
9	chr11:87224821-87224871	NB4	blood:	n/a
10	chr11:87204675-87204725	PANC-1	pancreas:	n/a
11	chr11:87224821-87224871	LNCaP	prostate:	n/a
12	chr11:87224821-87224871	SK-N-MC	brain:	n/a
13	chr11:87224821-87224871	NH-A	brain:	n/a
14	chr11:87224821-87224871	HEK293	kidney:	embryo
15	chr11:87224821-87224871	PFSK-1	brain:	n/a
16	chr11:87224821-87224871	HMEC	breast:	n/a
17	chr11:87224821-87224871	A549	lung:	n/a
18	chr11:87224821-87224871	AG10803	skin:	n/a
19	chr11:87204675-87204725	SAEC	small airway:	n/a
20	chr11:87204675-87204725	AG04450	lung:	fetal
21	chr11:87224821-87224871	SK-N-SH_RA	brain:	n/a
22	chr11:87224821-87224871	HepG2	liver:	n/a
23	chr11:87224821-87224871	BE2_C	brain:	n/a
24	chr11:87224821-87224871	H1-hESC	embryonic stem cell:	embryo
25	chr11:87204675-87204725	AG04449	skin:	fetal
26	chr11:87204675-87204725	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:87204675-87204725	MCF10A-Er-Src	breast:	n/a
28	chr11:87204675-87204725	HL-60	blood:	n/a
29	chr11:87224821-87224871	HCPEpiC	choroid plexus:	n/a
30	chr11:87204675-87204725	HepG2	liver:	n/a
31	chr11:87224821-87224871	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:87224821-87224871	AG09309	skin:	n/a
33	chr11:87204675-87204725	AG09319	gingival:	n/a
34	chr11:87204675-87204725	Caco-2	colon:	n/a
35	chr11:87224821-87224871	GM19239	blood:	n/a
36	chr11:87204675-87204725	BJ	skin:	n/a
37	chr11:87224821-87224871	MCF10A-Er-Src	breast:	n/a
38	chr11:87224821-87224871	HRPEpiC	eye:	n/a
39	chr11:87224821-87224871	IMR90	lung:	fetal
40	chr11:87204675-87204725	Hepatocyte	liver:	n/a
41	chr11:87224821-87224871	HUVEC	blood vessel:	n/a
42	chr11:87204675-87204725	AG09309	skin:	n/a
43	chr11:87224821-87224871	HRCEpiC	kidney:	n/a
44	chr11:87224821-87224871	GM06990	blood:	n/a
45	chr11:87224821-87224871	Jurkat	blood:	n/a
46	chr11:87204675-87204725	RPTEC	kidney:	n/a
47	chr11:87204675-87204725	PFSK-1	brain:	n/a
48	chr11:87204675-87204725	ProgFib	skin:	n/a
49	chr11:87204675-87204725	Jurkat	blood:	n/a
50	chr11:87224821-87224871	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr11:87197219..87198779-chr11:87200306..87201927,2	K562	blood:
2	chr11:87220063..87221996-chr11:87226594..87228726,2	K562	blood:
3	chr11:87197219..87198779-chr11:87200306..87201927,2	K562	blood:
4	chr11:87220063..87221996-chr11:87226594..87228726,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255391	TF binding region
ENSG00000255391	CpG island

Extended variants
information (count: 882 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11235162	chr11:87185278-87185279	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575008431	chr11:87185339-87185340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544027233	chr11:87185361-87185362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557259981	chr11:87185376-87185377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575775868	chr11:87185377-87185378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544661344	chr11:87185408-87185409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564551166	chr11:87185482-87185483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527261101	chr11:87185518-87185519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540950713	chr11:87185536-87185537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561265812	chr11:87185553-87185554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568370594	chr11:87185575-87185576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182761222	chr11:87185582-87185583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549990178	chr11:87185602-87185603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569747583	chr11:87185644-87185645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532661827	chr11:87185650-87185651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552668447	chr11:87185658-87185659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187475699	chr11:87185665-87185666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs193278170	chr11:87185701-87185702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17821940	chr11:87185714-87185715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568773281	chr11:87185771-87185772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114436747	chr11:87185818-87185819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575322151	chr11:87185836-87185837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368956847	chr11:87185842-87185843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4480570	chr11:87185843-87185844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114973724	chr11:87185848-87185849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576986319	chr11:87185861-87185862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183083012	chr11:87185880-87185881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187419717	chr11:87185884-87185885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544776559	chr11:87185890-87185891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571788330	chr11:87185891-87185892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541056196	chr11:87185921-87185922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560713573	chr11:87185922-87185923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530051105	chr11:87185926-87185927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543311194	chr11:87185948-87185949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563488054	chr11:87185961-87185962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532317245	chr11:87185992-87185993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552376839	chr11:87185993-87185994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7943190	chr11:87186005-87186006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs557506718	chr11:87186040-87186041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192066415	chr11:87186073-87186074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548608912	chr11:87186133-87186134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572963859	chr11:87186134-87186135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184156037	chr11:87186138-87186139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189763224	chr11:87186148-87186149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550961110	chr11:87186151-87186152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142664891	chr11:87186176-87186177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539675148	chr11:87186197-87186198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568557062	chr11:87186198-87186199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377089841	chr11:87186226-87186227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192461543	chr11:87186229-87186230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:87182200-87189000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:87183000-87185400	Enhancers	NHLF	lung
3	chr11:87183200-87185400	Enhancers	Osteobl	bone
4	chr11:87183600-87185400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:87185400-87187600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr11:87187600-87187800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:87187800-87188400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:87188400-87189200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:87189000-87189200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:87190600-87191000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:87195600-87195800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:87203400-87205400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:87203600-87204400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:87203800-87204400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr11:87203800-87204400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr11:87203800-87204400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:87203800-87205000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:87204000-87204400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr11:87204000-87205400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr11:87204200-87204400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:87204200-87204800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:87204200-87205200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr11:87204200-87205400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:87204400-87204600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr11:87204400-87204800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr11:87204400-87204800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr11:87204400-87204800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr11:87204400-87204800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr11:87204400-87205400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr11:87204400-87205600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr11:87204400-87205800	Enhancers	H9 Cell Line	embryonic stem cell
32	chr11:87204600-87204800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:87204600-87205000	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr11:87204600-87205200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:87204800-87205000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:87204800-87205400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr11:87204800-87205400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr11:87204800-87206200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr11:87204800-87207800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:87205000-87205200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr11:87205000-87205200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
42	chr11:87205000-87205200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr11:87205200-87205400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr11:87205200-87205800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr11:87205200-87206400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr11:87205400-87206600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr11:87205600-87206200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr11:87206200-87206400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr11:87206200-87207800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:87206400-87209400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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