Variant report

Variant	nsv909382
Chromosome Location	chr18:11870015-11892860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:550)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:11872545-11872809	HepG2	liver:	n/a	n/a
2	ATF2	chr18:11883094-11883544	GM12878	blood:	n/a	n/a
3	ATF2	chr18:11883120-11883477	GM12878	blood:	n/a	n/a
4	BATF	chr18:11883152-11883426	GM12878	blood:	n/a	n/a
5	BATF	chr18:11883128-11883508	GM12878	blood:	n/a	n/a
6	BATF	chr18:11887701-11887945	GM12878	blood:	n/a	chr18:11887841-11887852
7	BATF	chr18:11871500-11871846	GM12878	blood:	n/a	chr18:11871671-11871682
8	BATF	chr18:11871430-11871960	GM12878	blood:	n/a	chr18:11871671-11871682
9	BCL11A	chr18:11883181-11883384	GM12878	blood:	n/a	n/a
10	BCL11A	chr18:11871486-11871818	GM12878	blood:	n/a	chr18:11871704-11871713 chr18:11871671-11871680 chr18:11871670-11871679
11	BCLAF1	chr18:11883109-11883550	GM12878	blood:	n/a	n/a
12	BHLHE40	chr18:11880644-11881100	K562	blood:	n/a	n/a
13	BHLHE40	chr18:11872519-11872860	K562	blood:	n/a	n/a
14	BHLHE40	chr18:11872565-11872823	HepG2	liver:	n/a	n/a
15	BHLHE40	chr18:11883246-11883554	GM12878	blood:	n/a	n/a
16	BRCA1	chr18:11872598-11872764	HepG2	liver:	n/a	n/a
17	BRCA1	chr18:11887157-11888190	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr18:11872521-11872837	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr18:11875463-11875760	K562	blood:	n/a	n/a
20	CBX3	chr18:11875581-11875732	K562	blood:	n/a	n/a
21	CCNT2	chr18:11880603-11881137	K562	blood:	n/a	n/a
22	CCNT2	chr18:11887644-11888068	K562	blood:	n/a	chr18:11887656-11887676
23	CEBPB	chr18:11887409-11888106	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr18:11892509-11892758	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr18:11887558-11887995	MCF-7	breast:	n/a	n/a
26	CEBPB	chr18:11892559-11892698	K562	blood:	n/a	n/a
27	CEBPB	chr18:11869738-11870019	K562	blood:	n/a	chr18:11869858-11869869
28	CEBPB	chr18:11869690-11870054	K562	blood:	n/a	chr18:11869858-11869869
29	CEBPB	chr18:11892532-11892729	HepG2	liver:	n/a	n/a
30	CEBPD	chr18:11887552-11887975	K562	blood:	n/a	n/a
31	CEBPD	chr18:11880557-11881046	K562	blood:	n/a	n/a
32	CEBPD	chr18:11880493-11881089	K562	blood:	n/a	n/a
33	CHD2	chr18:11883208-11883502	GM12878	blood:	n/a	n/a
34	CHD2	chr18:11880690-11881045	K562	blood:	n/a	n/a
35	CHD2	chr18:11887572-11888111	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr18:11872620-11872770	GM12865	blood:	n/a	chr18:11872678-11872686
37	CTCF	chr18:11872583-11872788	GM19240	blood:	n/a	chr18:11872678-11872686
38	CTCF	chr18:11872556-11872821	HepG2	liver:	n/a	chr18:11872678-11872686
39	CTCF	chr18:11887400-11887550	HEK293	kidney:	n/a	n/a
40	CTCF	chr18:11874800-11874950	GM12865	blood:	n/a	chr18:11874843-11874851
41	CTCF	chr18:11872560-11872710	WI-38	lung:	n/a	chr18:11872678-11872686
42	CTCF	chr18:11872565-11872823	GM12892	blood:	n/a	chr18:11872678-11872686
43	CTCF	chr18:11872640-11872790	SAEC	small airway:	n/a	chr18:11872678-11872686
44	CTCF	chr18:11872559-11872825	LNCaP	prostate:	n/a	chr18:11872678-11872686
45	CTCF	chr18:11872573-11872789	GM19238	blood:	n/a	chr18:11872678-11872686
46	CTCF	chr18:11872600-11872750	HEEpiC	esophagus:	n/a	chr18:11872678-11872686
47	CTCF	chr18:11872700-11872850	WI-38	lung:	n/a	n/a
48	CTCF	chr18:11872600-11872750	HBMEC	blood vessel:	n/a	chr18:11872678-11872686
49	CTCF	chr18:11872640-11872790	GM06990	blood:	n/a	chr18:11872678-11872686
50	CTCF	chr18:11872504-11872967	MCF-7	breast:	n/a	chr18:11872678-11872686

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:11883985-11884035	SK-N-MC	brain:	n/a
2	chr18:11883985-11884035	SK-N-MC	brain:	n/a
3	chr18:11883985-11884035	PFSK-1	brain:	n/a
4	chr18:11881235-11881285	CMK	blood:	n/a
5	chr18:11881089-11881139	HCM	heart:	n/a
6	chr18:11881089-11881139	NHBE	bronchial:	n/a
7	chr18:11880973-11881023	Hela-S3	cervix:	n/a
8	chr18:11881235-11881285	SK-N-SH_RA	brain:	n/a
9	chr18:11884680-11884730	ProgFib	skin:	n/a
10	chr18:11880973-11881023	AG09309	skin:	n/a
11	chr18:11881089-11881139	Caco-2	colon:	n/a
12	chr18:11884680-11884730	AG04450	lung:	fetal
13	chr18:11881170-11881220	HNPCEpiC	eye:	n/a
14	chr18:11881089-11881139	SK-N-SH	brain:	n/a
15	chr18:11872908-11872958	K562	blood:	n/a
16	chr18:11883985-11884035	HepG2	liver:	n/a
17	chr18:11881089-11881139	NB4	blood:	n/a
18	chr18:11877637-11877687	HCM	heart:	n/a
19	chr18:11877637-11877687	ProgFib	skin:	n/a
20	chr18:11881235-11881285	AG09309	skin:	n/a
21	chr18:11881235-11881285	ovcar-3	ovarian:	n/a
22	chr18:11879979-11880029	PrEC	prostate:	n/a
23	chr18:11884680-11884730	AG09319	gingival:	n/a
24	chr18:11881170-11881220	Hela-S3	cervix:	n/a
25	chr18:11883985-11884035	GM06990	blood:	n/a
26	chr18:11881089-11881139	GM12891	blood:	n/a
27	chr18:11881089-11881139	SK-N-MC	brain:	n/a
28	chr18:11884680-11884730	HAEpiC	amniotic membrane:	n/a
29	chr18:11881089-11881139	A549	lung:	n/a
30	chr18:11881170-11881220	HepG2	liver:	n/a
31	chr18:11884680-11884730	ECC-1	luminal epithelium:	n/a
32	chr18:11881235-11881285	HRPEpiC	eye:	n/a
33	chr18:11883985-11884035	U87	brain:	n/a
34	chr18:11877637-11877687	SK-N-SH_RA	brain:	n/a
35	chr18:11880973-11881023	IMR90	lung:	fetal
36	chr18:11884680-11884730	IMR90	lung:	fetal
37	chr18:11884680-11884730	MCF10A-Er-Src	breast:	n/a
38	chr18:11880973-11881023	AG10803	skin:	n/a
39	chr18:11880973-11881023	ECC-1	luminal epithelium:	n/a
40	chr18:11881089-11881139	GM06990	blood:	n/a
41	chr18:11883985-11884035	CMK	blood:	n/a
42	chr18:11883985-11884035	BJ	skin:	n/a
43	chr18:11872908-11872958	PANC-1	pancreas:	n/a
44	chr18:11884680-11884730	NT2-D1	testis:	n/a
45	chr18:11881170-11881220	HCT-116	colon:	n/a
46	chr18:11881089-11881139	HMEC	breast:	n/a
47	chr18:11883985-11884035	HUVEC	blood vessel:	n/a
48	chr18:11877637-11877687	CMK	blood:	n/a
49	chr18:11881170-11881220	AoSMC	blood vessel:	n/a
50	chr18:11884680-11884730	HUVEC	blood vessel:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:11852115..11853636-chr18:11881450..11884165,2	K562	blood:
2	chr18:11886286..11887914-chr18:11890208..11892382,2	K562	blood:
3	chr18:11885563..11889310-chr18:11906331..11909961,4	MCF-7	breast:
4	chr18:11852816..11854453-chr18:11871185..11873560,2	MCF-7	breast:
5	chr18:11885013..11887914-chr18:11888832..11891708,3	K562	blood:
6	chr18:11732631..11733633-chr18:11872414..11873055,4	MCF-7	breast:
7	chr18:11885013..11887914-chr18:11888832..11891708,3	K562	blood:
8	chr18:11890272..11892139-chr18:11894063..11896941,2	MCF-7	breast:
9	chr18:11850832..11852430-chr18:11888810..11890757,2	K562	blood:
10	chr18:11882735..11885696-chr18:11887267..11889174,2	MCF-7	breast:
11	chr18:11655048..11655607-chr18:11872604..11873166,2	MCF-7	breast:
12	chr18:11892388..11894879-chr18:11897284..11900106,3	K562	blood:
13	chr18:11731021..11733810-chr18:11873223..11875083,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	GNAL	hsa-miR-16-5p	chr18:11881979-11881999
2	MPPE1	hsa-miR-101-3p	chr18:11884017-11884038
3	MPPE1	hsa-miR-101-3p	chr18:11884274-11884292

Variant related genes	Relation type
GNAL	TF binding region
MPPE1	TF binding region
GNAL	CpG island
MPPE1	CpG island
ENSG00000255112	chromatin interactions
ENSG00000267165	chromatin interactions
ENSG00000154889	chromatin interactions
ENSG00000273141	chromatin interactions

Extended variants
information (count: 1276 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1276 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2848463	chr18:11870015-11870016	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571126715	chr18:11870055-11870056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527388675	chr18:11870062-11870063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2855649	chr18:11870071-11870072	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs112450669	chr18:11870089-11870090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560854875	chr18:11870104-11870105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566474083	chr18:11870133-11870134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550440117	chr18:11870154-11870155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550075785	chr18:11870156-11870157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs151206935	chr18:11870194-11870195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12454628	chr18:11870225-11870226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183531480	chr18:11870233-11870234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375796291	chr18:11870259-11870260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9947329	chr18:11870294-11870295	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs373424323	chr18:11870297-11870298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534025059	chr18:11870341-11870342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374249199	chr18:11870368-11870369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12454601	chr18:11870377-11870378	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113710016	chr18:11870379-11870380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567301738	chr18:11870393-11870394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9947591	chr18:11870434-11870435	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs188074545	chr18:11870444-11870445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552550300	chr18:11870445-11870446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201313704	chr18:11870527-11870528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111765820	chr18:11870532-11870533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9947607	chr18:11870537-11870538	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535445508	chr18:11870538-11870539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140919851	chr18:11870552-11870553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377730837	chr18:11870553-11870554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201160158	chr18:11870563-11870564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572721888	chr18:11870591-11870592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542726680	chr18:11870607-11870608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143597070	chr18:11870649-11870650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557731122	chr18:11870650-11870651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180977432	chr18:11870700-11870701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144943637	chr18:11870701-11870702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185443171	chr18:11870702-11870703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565145828	chr18:11870704-11870705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191371673	chr18:11870705-11870706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181612726	chr18:11870708-11870709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559273163	chr18:11870714-11870715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529867291	chr18:11870722-11870723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566533451	chr18:11870725-11870726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74342890	chr18:11870741-11870742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2848464	chr18:11870805-11870806	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs537810348	chr18:11870830-11870831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549913431	chr18:11870847-11870848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571664775	chr18:11870891-11870892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139016714	chr18:11870904-11870905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374285131	chr18:11870909-11870910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:718 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:11852400-11880800	Weak transcription	Aorta	Aorta
2	chr18:11853600-11883800	Weak transcription	Ovary	ovary
3	chr18:11853800-11884200	Weak transcription	Brain Substantia Nigra	brain
4	chr18:11854000-11875000	Weak transcription	Brain Hippocampus Middle	brain
5	chr18:11854000-11884200	Weak transcription	Brain Angular Gyrus	brain
6	chr18:11854800-11889200	Weak transcription	Fetal Brain Male	brain
7	chr18:11855400-11875400	Weak transcription	Fetal Stomach	stomach
8	chr18:11855600-11880800	Weak transcription	Fetal Brain Female	brain
9	chr18:11857600-11872800	Weak transcription	Left Ventricle	heart
10	chr18:11857800-11875200	Weak transcription	Brain Germinal Matrix	brain
11	chr18:11857800-11876400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr18:11858200-11884000	Weak transcription	Colon Smooth Muscle	Colon
13	chr18:11858600-11875800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr18:11858600-11879400	Weak transcription	Adipose Nuclei	Adipose
15	chr18:11859000-11886400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr18:11859200-11875600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr18:11860200-11875200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr18:11860200-11875400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr18:11861000-11880800	Weak transcription	Esophagus	oesophagus
20	chr18:11861600-11873400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr18:11861800-11872600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr18:11861800-11887800	Weak transcription	Psoas Muscle	Psoas
23	chr18:11862400-11871400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr18:11862400-11879200	Weak transcription	Spleen	Spleen
25	chr18:11862600-11872000	Weak transcription	Hela-S3	cervix
26	chr18:11865000-11870200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr18:11865400-11874200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr18:11865800-11872400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr18:11866400-11873400	Weak transcription	Stomach Smooth Muscle	stomach
30	chr18:11867000-11872800	Weak transcription	Brain Anterior Caudate	brain
31	chr18:11867200-11884000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr18:11867200-11884400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr18:11867400-11880800	Weak transcription	Duodenum Mucosa	Duodenum
34	chr18:11868200-11870200	Strong transcription	Skeletal Muscle Male	skeletal muscle
35	chr18:11868200-11870200	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr18:11868200-11875400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr18:11868400-11870200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr18:11868600-11873600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr18:11868800-11873400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:11868800-11877600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr18:11869000-11874000	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr18:11869000-11875600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr18:11869000-11876000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr18:11869000-11877800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr18:11869000-11877800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr18:11869600-11871600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr18:11870200-11871800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr18:11870200-11872400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr18:11870200-11872600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr18:11870200-11872600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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