Variant report

Variant	nsv891261
Chromosome Location	chr8:106880649-106932634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:106909436-106909708	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:106918074-106918917	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:106920550-106920657	K562	blood:	n/a	n/a
4	BRCA1	chr8:106884105-106884177	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr8:106914661-106915099	K562	blood:	n/a	n/a
6	CBX3	chr8:106929016-106929303	K562	blood:	n/a	n/a
7	CBX3	chr8:106930473-106930765	K562	blood:	n/a	n/a
8	CEBPB	chr8:106930362-106930587	A549	lung:	n/a	n/a
9	CEBPB	chr8:106930368-106930574	IMR90	lung:	n/a	n/a
10	CHD2	chr8:106909456-106909643	HepG2	liver:	n/a	n/a
11	CREB1	chr8:106920540-106920825	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr8:106920428-106920900	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:106918180-106918330	GM12801	blood:	n/a	chr8:106918284-106918305 chr8:106918282-106918300 chr8:106918283-106918299 chr8:106918285-106918298
14	CTCF	chr8:106906920-106907070	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr8:106920560-106920710	GM12867	blood:	n/a	n/a
16	CTCF	chr8:106918740-106918890	AG04450	lung:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
17	CTCF	chr8:106920580-106920730	GM12867	blood:	n/a	n/a
18	CTCF	chr8:106918724-106918933	GM13977	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
19	CTCF	chr8:106918300-106918450	NHLF	lung:	n/a	n/a
20	CTCF	chr8:106920560-106920710	HFF	foreskin:	n/a	n/a
21	CTCF	chr8:106920520-106920670	AG04450	lung:	n/a	n/a
22	CTCF	chr8:106918240-106918390	HVMF	connective:	n/a	chr8:106918284-106918305 chr8:106918282-106918300 chr8:106918283-106918299 chr8:106918285-106918298
23	CTCF	chr8:106898714-106898749	ProgFib	skin:	n/a	n/a
24	CTCF	chr8:106918700-106918850	GM12865	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
25	CTCF	chr8:106918740-106918890	HL-60	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
26	CTCF	chr8:106920580-106920730	GM12878	blood:	n/a	n/a
27	CTCF	chr8:106920600-106920750	GM12872	blood:	n/a	n/a
28	CTCF	chr8:106918141-106918429	SK-N-SH_RA	brain:	n/a	chr8:106918284-106918305 chr8:106918282-106918300 chr8:106918283-106918299 chr8:106918285-106918298
29	CTCF	chr8:106920560-106920710	AG04449	skin:	n/a	n/a
30	CTCF	chr8:106920580-106920730	GM12864	blood:	n/a	n/a
31	CTCF	chr8:106920337-106921019	SK-N-SH	brain:	n/a	n/a
32	CTCF	chr8:106920560-106920710	GM12868	blood:	n/a	n/a
33	CTCF	chr8:106918240-106918390	HMF	breast:	n/a	chr8:106918284-106918305 chr8:106918282-106918300 chr8:106918283-106918299 chr8:106918285-106918298
34	CTCF	chr8:106918708-106918973	A549	lung:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
35	CTCF	chr8:106917800-106917950	GM12865	blood:	n/a	n/a
36	CTCF	chr8:106918720-106918870	GM12874	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
37	CTCF	chr8:106920504-106920761	HepG2	liver:	n/a	n/a
38	CTCF	chr8:106920960-106921110	HCFaa	heart:	n/a	n/a
39	CTCF	chr8:106918760-106918910	GM12871	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
40	CTCF	chr8:106909877-106909955	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:106917700-106917850	WI-38	lung:	n/a	n/a
42	CTCF	chr8:106918700-106918850	GM12873	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918824-106918845
43	CTCF	chr8:106917720-106917870	HFF	foreskin:	n/a	n/a
44	CTCF	chr8:106918057-106919004	K562	blood:	n/a	chr8:106918822-106918840 chr8:106918823-106918839 chr8:106918284-106918305 chr8:106918825-106918838 chr8:106918825-106918834 chr8:106918282-106918300 chr8:106918283-106918299 chr8:106918285-106918298 chr8:106918824-106918845
45	CTCF	chr8:106918200-106918350	HBMEC	blood vessel:	n/a	chr8:106918284-106918305 chr8:106918282-106918300 chr8:106918283-106918299 chr8:106918285-106918298
46	CTCF	chr8:106920349-106920940	HCT-116	colon:	n/a	n/a
47	CTCF	chr8:106920560-106920710	A549	lung:	n/a	n/a
48	CTCF	chr8:106920563-106920735	GM20000	blood:	n/a	n/a
49	CTCF	chr8:106917640-106917790	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr8:106918320-106918470	GM12870	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:106917865..106918639-chr8:106952052..106952798,2	MCF-7	breast:
2	chr8:106917848..106919209-chr8:107533760..107534650,3	MCF-7	breast:
3	chr16:10785707..10786527-chr8:106898296..106899109,2	MCF-7	breast:
4	chr8:106919536..106922132-chr8:106923393..106927585,4	K562	blood:
5	chr8:106918347..106919345-chr8:107093305..107094021,2	MCF-7	breast:
6	chr8:106793582..106794628-chr8:106918021..106919265,4	MCF-7	breast:
7	chr8:106917185..106917788-chr8:107603831..107604640,2	MCF-7	breast:
8	chr8:106915226..106916860-chr8:106919746..106922369,2	MCF-7	breast:
9	chr8:106918427..106919291-chr8:107205443..107205988,2	MCF-7	breast:
10	chr8:106932622..106934542-chr8:106950174..106953659,3	K562	blood:
11	chr8:106876622..106878636-chr8:106878865..106881830,2	K562	blood:
12	chr8:106894712..106896859-chr8:106900019..106901770,2	K562	blood:
13	chr8:106920579..106921125-chr8:107016679..107017190,2	MCF-7	breast:
14	chr8:106915226..106916860-chr8:106919746..106922369,2	MCF-7	breast:
15	chr8:106918479..106919292-chr8:107603720..107604631,2	MCF-7	breast:
16	chr8:106920154..106920891-chr8:107603707..107604258,2	K562	blood:
17	chr8:106793666..106794620-chr8:106918373..106919405,3	MCF-7	breast:
18	chr8:106894712..106896859-chr8:106900019..106901770,2	K562	blood:
19	chr8:106920159..106921437-chr8:107603839..107604727,4	MCF-7	breast:
20	chr8:106917815..106919520-chr8:107603747..107605061,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFPM2-3	chr8:106915584-106915799	NONHSAT128245
2	lnc-RP11-778D12.2.1-4	chr8:106924033-106924097	ENSG00000251003.2
3	lnc-ZFPM2-2	chr8:106891248-106891477	NONHSAT128244

Variant related genes	Relation type
ENSG00000251003	TF binding region
ENSG00000251003	chromatin interactions

Extended variants
information (count: 1436 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1436 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148067142	chr8:106884050-106884051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547221361	chr8:106884064-106884065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577552661	chr8:106884086-106884087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571836406	chr8:106884094-106884095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142647294	chr8:106884132-106884133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557232364	chr8:106884133-106884134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370536666	chr8:106884146-106884147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146019562	chr8:106884147-106884148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374254432	chr8:106884163-106884164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200660289	chr8:106884164-106884165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139823474	chr8:106884213-106884214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548217094	chr8:106884259-106884260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573314064	chr8:106884342-106884343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540050501	chr8:106884343-106884344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368459019	chr8:106884362-106884363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183064510	chr8:106884364-106884365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185391577	chr8:106884401-106884402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544491457	chr8:106884408-106884409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11776605	chr8:106884436-106884437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374550628	chr8:106884438-106884439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35736826	chr8:106884443-106884444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143114608	chr8:106884457-106884458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560929744	chr8:106884470-106884471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540117750	chr8:106884500-106884501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189990625	chr8:106884560-106884561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575794383	chr8:106884564-106884565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560342515	chr8:106884589-106884590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73698349	chr8:106884616-106884617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182197755	chr8:106884666-106884667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12550560	chr8:106884685-106884686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs551993258	chr8:106884687-106884688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372654999	chr8:106884735-106884736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571764312	chr8:106884787-106884788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146215717	chr8:106884878-106884879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550826772	chr8:106884888-106884889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569243685	chr8:106884925-106884926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371991340	chr8:106885030-106885031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72081728	chr8:106885031-106885032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4036802	chr8:106885058-106885059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371466828	chr8:106885102-106885103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139088249	chr8:106885153-106885154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554590696	chr8:106885188-106885189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376373839	chr8:106885189-106885190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs59757927	chr8:106885219-106885220	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs534910476	chr8:106885259-106885260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534251145	chr8:106885311-106885312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558804863	chr8:106885384-106885385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576933290	chr8:106885401-106885402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544452331	chr8:106885425-106885426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556473336	chr8:106885465-106885466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106884000-106884200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:106884200-106885600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:106885400-106885800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:106885600-106886000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr8:106885600-106886200	Enhancers	Thymus	Thymus
6	chr8:106885600-106886400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:106885600-106886400	Enhancers	Fetal Thymus	thymus
8	chr8:106885600-106886800	Enhancers	NHEK	skin
9	chr8:106885600-106887000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:106886000-106886600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:106886200-106886600	Enhancers	HMEC	breast
12	chr8:106886200-106886800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr8:106886400-106886800	Enhancers	NHDF-Ad	bronchial
14	chr8:106886400-106887000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:106888000-106888200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:106888200-106888600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:106893400-106895800	Weak transcription	Hela-S3	cervix
18	chr8:106893800-106894200	Active TSS	Gastric	stomach
19	chr8:106894000-106894400	Enhancers	Fetal Intestine Small	intestine
20	chr8:106895400-106896200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:106895800-106896400	Enhancers	Hela-S3	cervix
22	chr8:106895800-106896400	Enhancers	NH-A	brain
23	chr8:106896000-106896800	Enhancers	Osteobl	bone
24	chr8:106896200-106896400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:106896200-106896400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:106896200-106896400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:106896200-106896400	Enhancers	Fetal Muscle Leg	muscle
28	chr8:106896400-106897400	Weak transcription	NH-A	brain
29	chr8:106896400-106897600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr8:106896400-106897600	Weak transcription	Fetal Muscle Leg	muscle
31	chr8:106896400-106898600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr8:106896600-106897600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr8:106896800-106897200	Weak transcription	Osteobl	bone
34	chr8:106897200-106898000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr8:106897200-106898600	Enhancers	Osteobl	bone
36	chr8:106897400-106898000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:106897400-106898400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:106897400-106898800	Enhancers	NH-A	brain
39	chr8:106897600-106898200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr8:106897600-106898600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr8:106897600-106898800	Enhancers	Fetal Muscle Leg	muscle
42	chr8:106897800-106898400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:106897800-106899000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:106898600-106899000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:106899000-106899200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr8:106899000-106899200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:106899000-106899800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:106899200-106909000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:106899400-106899800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:106907000-106908200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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