Variant report

Variant	nsv517681
Chromosome Location	chr10:96343228-96387079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:309)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:96351416-96352277	GM12878	blood:	n/a	n/a
2	ATF2	chr10:96366792-96367363	GM12878	blood:	n/a	n/a
3	ATF2	chr10:96351445-96352076	GM12878	blood:	n/a	n/a
4	ATF2	chr10:96366761-96367462	GM12878	blood:	n/a	n/a
5	ATF2	chr10:96383262-96383689	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:96351342-96352046	GM12878	blood:	n/a	n/a
7	BATF	chr10:96351300-96352091	GM12878	blood:	n/a	n/a
8	BATF	chr10:96366750-96367381	GM12878	blood:	n/a	chr10:96367154-96367163 chr10:96367048-96367059
9	BATF	chr10:96366796-96367376	GM12878	blood:	n/a	chr10:96367154-96367163 chr10:96367048-96367059
10	BCL11A	chr10:96351507-96352049	GM12878	blood:	n/a	chr10:96351584-96351591
11	BCL11A	chr10:96366874-96367200	GM12878	blood:	n/a	n/a
12	BCL11A	chr10:96383339-96383553	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr10:96366831-96367311	GM12878	blood:	n/a	n/a
14	BCL3	chr10:96351574-96351893	GM12878	blood:	n/a	chr10:96351584-96351591
15	BCL3	chr10:96366592-96367340	GM12878	blood:	n/a	n/a
16	BCLAF1	chr10:96366730-96367340	GM12878	blood:	n/a	n/a
17	BCLAF1	chr10:96366732-96367283	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:96351363-96351973	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:96366743-96367284	GM12878	blood:	n/a	n/a
20	BRCA1	chr10:96368202-96368280	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:96351468-96352119	GM12878	blood:	n/a	n/a
22	CEBPB	chr10:96369983-96370337	ECC-1	luminal epithelium:	n/a	n/a
23	CHD1	chr10:96367282-96367348	GM12878	blood:	n/a	n/a
24	CHD2	chr10:96351456-96351908	GM12878	blood:	n/a	n/a
25	CREB1	chr10:96351469-96352119	GM12878	blood:	n/a	n/a
26	CTCF	chr10:96345034-96345207	K562	blood:	n/a	n/a
27	CTCF	chr10:96379278-96379329	LNCaP	prostate:	n/a	n/a
28	CTCF	chr10:96345214-96345259	GM13976	blood:	n/a	n/a
29	CTCF	chr10:96345037-96345358	K562	blood:	n/a	n/a
30	CTCF	chr10:96362200-96362350	HCPEpiC	choroid plexus:	n/a	n/a
31	CUX1	chr10:96366863-96367388	GM12878	blood:	n/a	n/a
32	CUX1	chr10:96351123-96352287	GM12878	blood:	n/a	n/a
33	E2F4	chr10:96355957-96356237	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr10:96366720-96367380	GM12878	blood:	n/a	n/a
35	EBF1	chr10:96351207-96351967	GM12878	blood:	n/a	chr10:96351414-96351425
36	EBF1	chr10:96351278-96351584	GM12878	blood:	n/a	chr10:96351414-96351425
37	EBF1	chr10:96351167-96351572	GM12878	blood:	n/a	chr10:96351414-96351425
38	ELK1	chr10:96351712-96351984	GM12878	blood:	n/a	n/a
39	EP300	chr10:96342958-96343256	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr10:96351319-96351991	GM12878	blood:	n/a	chr10:96351933-96351943
41	EP300	chr10:96366756-96367282	GM12878	blood:	n/a	n/a
42	EP300	chr10:96366829-96367330	GM12878	blood:	n/a	n/a
43	EP300	chr10:96366904-96367268	GM12878	blood:	n/a	n/a
44	EP300	chr10:96351246-96352103	GM12878	blood:	n/a	chr10:96351933-96351943
45	EP300	chr10:96351375-96352039	GM12878	blood:	n/a	chr10:96351933-96351943
46	EP300	chr10:96383234-96383650	H1-hESC	embryonic stem cell:	n/a	n/a
47	FOS	chr10:96379047-96379078	MCF10A-Er-Src	breast:	n/a	n/a
48	FOXA1	chr10:96343658-96343967	T-47D	breast:	n/a	n/a
49	FOXA1	chr10:96343572-96344034	T-47D	breast:	n/a	chr10:96343992-96344004
50	FOXA2	chr10:96345015-96345294	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96383628-96383678	T-47D	breast:	n/a
2	chr10:96383628-96383678	NB4	blood:	n/a
3	chr10:96383628-96383678	Jurkat	blood:	n/a
4	chr10:96383628-96383678	ProgFib	skin:	n/a
5	chr10:96383628-96383678	AG04450	lung:	fetal
6	chr10:96383628-96383678	SAEC	small airway:	n/a
7	chr10:96383628-96383678	GM12891	blood:	n/a
8	chr10:96383628-96383678	IMR90	lung:	fetal
9	chr10:96383628-96383678	BJ	skin:	n/a
10	chr10:96383628-96383678	LNCaP	prostate:	n/a
11	chr10:96383628-96383678	HEK293	kidney:	embryo
12	chr10:96383628-96383678	HCF	heart:	n/a
13	chr10:96383628-96383678	HAEpiC	amniotic membrane:	n/a
14	chr10:96383628-96383678	AG10803	skin:	n/a
15	chr10:96383628-96383678	ECC-1	luminal epithelium:	n/a
16	chr10:96383628-96383678	Caco-2	colon:	n/a
17	chr10:96383628-96383678	Hepatocyte	liver:	n/a
18	chr10:96383628-96383678	GM06990	blood:	n/a
19	chr10:96383628-96383678	ovcar-3	ovarian:	n/a
20	chr10:96383628-96383678	BE2_C	brain:	n/a
21	chr10:96383628-96383678	HCM	heart:	n/a
22	chr10:96383628-96383678	HPAEpiC	pulmonary alveolar:	n/a
23	chr10:96383628-96383678	HepG2	liver:	n/a
24	chr10:96383628-96383678	AG09319	gingival:	n/a
25	chr10:96383628-96383678	SKMC	muscle:	n/a
26	chr10:96383628-96383678	AoSMC	blood vessel:	n/a
27	chr10:96383628-96383678	RPTEC	kidney:	n/a
28	chr10:96383628-96383678	HCT-116	colon:	n/a
29	chr10:96383628-96383678	HMEC	breast:	n/a
30	chr10:96383628-96383678	NH-A	brain:	n/a
31	chr10:96383628-96383678	K562	blood:	n/a
32	chr10:96383628-96383678	GM12878	blood:	n/a
33	chr10:96383628-96383678	HIPEpiC	eye:	n/a
34	chr10:96383628-96383678	HNPCEpiC	eye:	n/a
35	chr10:96383628-96383678	SK-N-SH_RA	brain:	n/a
36	chr10:96383628-96383678	GM19239	blood:	n/a
37	chr10:96383628-96383678	HRPEpiC	eye:	n/a
38	chr10:96383628-96383678	AG09309	skin:	n/a
39	chr10:96383628-96383678	A549	lung:	n/a
40	chr10:96383628-96383678	PANC-1	pancreas:	n/a
41	chr10:96383628-96383678	NHDF-neo	bronchial:	n/a
42	chr10:96383628-96383678	PrEC	prostate:	n/a
43	chr10:96383628-96383678	HL-60	blood:	n/a
44	chr10:96383628-96383678	NT2-D1	testis:	n/a
45	chr10:96383628-96383678	PFSK-1	brain:	n/a
46	chr10:96383628-96383678	MCF-7	breast:	n/a
47	chr10:96383628-96383678	HRE	kidney:	n/a
48	chr10:96383628-96383678	H1-hESC	embryonic stem cell:	embryo
49	chr10:96383628-96383678	SK-N-SH	brain:	n/a
50	chr10:96383628-96383678	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:96339432..96341136-chr10:96352569..96355112,2	K562	blood:
2	chr10:96352629..96354716-chr10:96356087..96359536,3	K562	blood:
3	chr10:96346410..96347997-chr10:96362678..96364645,2	K562	blood:
4	chr10:96372045..96374578-chr10:96375637..96378833,3	K562	blood:
5	chr10:96364298..96366662-chr10:96373038..96375239,3	K562	blood:
6	chr10:96313161..96315470-chr10:96353062..96355863,2	K562	blood:
7	chr10:96364298..96366662-chr10:96373038..96375239,3	K562	blood:
8	chr10:96361276..96363371-chr10:96363793..96366493,2	K562	blood:
9	chr10:96372045..96374578-chr10:96375637..96378833,3	K562	blood:
10	chr10:96346410..96347997-chr10:96362678..96364645,2	K562	blood:
11	chr10:96384761..96386735-chr10:96941217..96943673,2	MCF-7	breast:
12	chr10:96361276..96363371-chr10:96363793..96366493,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D12-1	chr10:96370558-96370995	ENSG00000244332.1
2	lnc-CYP2C18-1	chr10:96372044-96373661	NONHSAT015736

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HELLS	hsa-miR-7-5p	chr10:96361638-96361661
2	HELLS	hsa-miR-7-5p	chr10:96361654-96361660

Variant related genes	Relation type
HELLS	TF binding region
HELLS	CpG island
ENSG00000119969	chromatin interactions
ENSG00000225533	chromatin interactions

Extended variants
information (count: 1724 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4918409	chr10:96343228-96343229	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534745123	chr10:96343236-96343237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370131628	chr10:96343298-96343299	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554523343	chr10:96343312-96343313	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117843577	chr10:96343358-96343359	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537362311	chr10:96343374-96343375	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188410707	chr10:96343399-96343400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565093466	chr10:96343410-96343411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200428876	chr10:96343461-96343462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142229138	chr10:96343468-96343469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577368697	chr10:96343472-96343473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546037728	chr10:96343481-96343482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553071780	chr10:96343520-96343521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112286673	chr10:96343617-96343618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146238737	chr10:96343620-96343621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs962234	chr10:96343623-96343624	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530491851	chr10:96343628-96343629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544522140	chr10:96343634-96343635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184515873	chr10:96343649-96343650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564185698	chr10:96343664-96343665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201120008	chr10:96343673-96343674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533195517	chr10:96343679-96343680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75419281	chr10:96343699-96343700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12355288	chr10:96343733-96343734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566195266	chr10:96343836-96343837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543533134	chr10:96343911-96343912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528550872	chr10:96343914-96343915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548245039	chr10:96343955-96343956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76907176	chr10:96343979-96343980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188962401	chr10:96344024-96344025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536998710	chr10:96344054-96344055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115491363	chr10:96344085-96344086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571047432	chr10:96344114-96344115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552975271	chr10:96344117-96344118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192350150	chr10:96344175-96344176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117574153	chr10:96344199-96344200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553268671	chr10:96344306-96344307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74150834	chr10:96344331-96344332	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs35665202	chr10:96344362-96344363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77320190	chr10:96344403-96344404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185766485	chr10:96344445-96344446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533800953	chr10:96344448-96344449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7068337	chr10:96344458-96344459	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs575321528	chr10:96344476-96344477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149253192	chr10:96344509-96344510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543855617	chr10:96344539-96344540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143490674	chr10:96344597-96344598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189077548	chr10:96344602-96344603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372096540	chr10:96344652-96344653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540457118	chr10:96344657-96344658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96306400-96357200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:96306400-96365600	Weak transcription	Esophagus	oesophagus
3	chr10:96306400-96370400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr10:96306400-96370600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr10:96306400-96371000	Weak transcription	Ovary	ovary
6	chr10:96306600-96349800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr10:96306600-96353800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr10:96306600-96379200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:96306800-96348000	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr10:96306800-96348200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr10:96306800-96348400	Weak transcription	Primary B cells from cord blood	blood
12	chr10:96306800-96349800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr10:96306800-96357200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr10:96306800-96373000	Weak transcription	Primary T cells from cord blood	blood
15	chr10:96307000-96358200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:96307000-96375000	Weak transcription	Osteobl	bone
17	chr10:96307200-96371200	Weak transcription	Fetal Brain Male	brain
18	chr10:96307600-96356000	Weak transcription	NHDF-Ad	bronchial
19	chr10:96307600-96373200	Weak transcription	Brain Germinal Matrix	brain
20	chr10:96307800-96348200	Weak transcription	NHEK	skin
21	chr10:96307800-96373000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr10:96308000-96373200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:96309400-96354000	Weak transcription	K562	blood
24	chr10:96309600-96372800	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr10:96309600-96377000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr10:96312200-96354000	Weak transcription	Gastric	stomach
27	chr10:96312800-96372200	Strong transcription	Dnd41	blood
28	chr10:96314200-96373400	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr10:96315000-96369200	Weak transcription	Fetal Kidney	kidney
30	chr10:96315600-96343800	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr10:96315600-96345200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:96316000-96371400	Weak transcription	Fetal Brain Female	brain
33	chr10:96316000-96374000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr10:96316200-96357600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr10:96316200-96373000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr10:96317000-96372600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr10:96317400-96348000	Weak transcription	NH-A	brain
38	chr10:96321000-96353200	Weak transcription	Fetal Intestine Large	intestine
39	chr10:96324000-96356600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr10:96324000-96376600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr10:96324200-96353800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr10:96324200-96365600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr10:96325800-96348200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:96325800-96376000	Weak transcription	NHLF	lung
45	chr10:96327000-96347400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr10:96327800-96348000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr10:96330200-96348000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr10:96330600-96347800	Weak transcription	HUVEC	blood vessel
49	chr10:96331000-96377400	Weak transcription	Placenta	Placenta
50	chr10:96331200-96361800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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