Variant report

Variant	nsv8037
Chromosome Location	chr7:6010076-6018230
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:196)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:196 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:6010851-6011025	MCF-7	breast:	n/a	n/a
2	CTCF	chr7:6010858-6011010	MCF-7	breast:	n/a	n/a
3	CTCF	chr7:6010895-6011014	GM19238	blood:	n/a	n/a
4	CTCF	chr7:6010857-6010973	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr7:6010865-6010990	HepG2	liver:	n/a	n/a
6	CTCF	chr7:6010848-6011022	MCF-7	breast:	n/a	n/a
7	CTCF	chr7:6016137-6016265	GM12891	blood:	n/a	n/a
8	CTCF	chr7:6010884-6010989	GM12891	blood:	n/a	n/a
9	CTCF	chr7:6011709-6011764	GM12891	blood:	n/a	n/a
10	CTCF	chr7:6010878-6011009	GM12892	blood:	n/a	n/a
11	CTCF	chr7:6010868-6011012	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:6010872-6011024	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr7:6010845-6010990	NHEK	skin:	n/a	n/a
14	CTCF	chr7:6010905-6010978	Gliobla	brain:	n/a	n/a
15	CTCF	chr7:6016168-6016291	GM19239	blood:	n/a	n/a
16	CTCF	chr7:6010838-6011005	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr7:6010875-6010995	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:6010890-6010913	Lung_OC	lung:	n/a	n/a
19	CTCF	chr7:6010897-6010968	GM19239	blood:	n/a	n/a
20	CTCF	chr7:6010844-6010977	K562	blood:	n/a	n/a
21	CTCF	chr7:6010843-6010922	GM19240	blood:	n/a	n/a
22	CTCF	chr7:6010900-6010922	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr7:6010912-6010977	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr7:6010874-6010966	GM12878	blood:	n/a	n/a
25	FOSL2	chr7:6010019-6010528	HepG2	liver:	n/a	n/a
26	FOSL2	chr7:6010850-6011171	HepG2	liver:	n/a	n/a
27	MYC	chr7:6016145-6016213	MCF-7	breast:	n/a	n/a
28	MYC	chr7:6013579-6013700	MCF-7	breast:	n/a	n/a
29	MYC	chr7:6016100-6016268	MCF-7	breast:	n/a	chr7:6016210-6016219 chr7:6016211-6016218
30	MYC	chr7:6014920-6014939	MCF-7	breast:	n/a	n/a
31	MYC	chr7:6012192-6012226	HUVEC	blood vessel:	n/a	n/a
32	MYC	chr7:6014164-6014299	MCF-7	breast:	n/a	n/a
33	MYC	chr7:6013652-6013722	MCF-7	breast:	n/a	n/a
34	MYC	chr7:6013565-6013575	MCF-7	breast:	n/a	n/a
35	MYC	chr7:6010082-6010150	HUVEC	blood vessel:	n/a	n/a
36	PAX5	chr7:6010084-6010457	GM12878	blood:	n/a	n/a
37	POLR2A	chr7:6010997-6011211	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr7:6016105-6016227	MCF-7	breast:	n/a	n/a
39	POLR2A	chr7:6011604-6011898	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr7:6009593-6010810	SK-N-MC	brain:	n/a	n/a
41	POLR2A	chr7:6014922-6014985	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr7:6012141-6012184	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr7:6014965-6014969	MCF-7	breast:	n/a	n/a
44	POLR2A	chr7:6011745-6011767	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr7:6011641-6011997	GM12878	blood:	n/a	n/a
46	POLR2A	chr7:6010002-6010499	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr7:6009974-6010506	GM12878	blood:	n/a	n/a
48	POLR2A	chr7:6011897-6012133	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr7:6011100-6011139	MCF-7	breast:	n/a	n/a
50	POLR2A	chr7:6010274-6010798	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6014034-6014084	NHBE	bronchial:	n/a
2	chr7:6010084-6010134	HNPCEpiC	eye:	n/a
3	chr7:6010084-6010134	Hepatocyte	liver:	n/a
4	chr7:6010084-6010134	H1-hESC	embryonic stem cell:	embryo
5	chr7:6010084-6010134	RPTEC	kidney:	n/a
6	chr7:6014034-6014084	RPTEC	kidney:	n/a
7	chr7:6010084-6010134	BE2_C	brain:	n/a
8	chr7:6014034-6014084	PANC-1	pancreas:	n/a
9	chr7:6014034-6014084	AG10803	skin:	n/a
10	chr7:6014034-6014084	GM06990	blood:	n/a
11	chr7:6010084-6010134	PrEC	prostate:	n/a
12	chr7:6010084-6010134	HRE	kidney:	n/a
13	chr7:6010084-6010134	ECC-1	luminal epithelium:	n/a
14	chr7:6014034-6014084	SK-N-SH	brain:	n/a
15	chr7:6010084-6010134	Hela-S3	cervix:	n/a
16	chr7:6014034-6014084	IMR90	lung:	fetal
17	chr7:6010084-6010134	T-47D	breast:	n/a
18	chr7:6010084-6010134	GM12878	blood:	n/a
19	chr7:6010084-6010134	HL-60	blood:	n/a
20	chr7:6014034-6014084	SK-N-MC	brain:	n/a
21	chr7:6014034-6014084	GM12892	blood:	n/a
22	chr7:6010084-6010134	NHDF-neo	bronchial:	n/a
23	chr7:6014034-6014084	NB4	blood:	n/a
24	chr7:6010084-6010134	ovcar-3	ovarian:	n/a
25	chr7:6014034-6014084	GM12891	blood:	n/a
26	chr7:6014034-6014084	Caco-2	colon:	n/a
27	chr7:6010084-6010134	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:6010084-6010134	LNCaP	prostate:	n/a
29	chr7:6014034-6014084	GM19239	blood:	n/a
30	chr7:6010084-6010134	NHBE	bronchial:	n/a
31	chr7:6014034-6014084	Hela-S3	cervix:	n/a
32	chr7:6010084-6010134	GM06990	blood:	n/a
33	chr7:6014034-6014084	AoSMC	blood vessel:	n/a
34	chr7:6014034-6014084	HCT-116	colon:	n/a
35	chr7:6010084-6010134	MCF-7	breast:	n/a
36	chr7:6010084-6010134	HepG2	liver:	n/a
37	chr7:6010084-6010134	GM19239	blood:	n/a
38	chr7:6014034-6014084	HEK293	kidney:	embryo
39	chr7:6014034-6014084	Jurkat	blood:	n/a
40	chr7:6010084-6010134	NT2-D1	testis:	n/a
41	chr7:6014034-6014084	CMK	blood:	n/a
42	chr7:6010084-6010134	HCM	heart:	n/a
43	chr7:6014034-6014084	NH-A	brain:	n/a
44	chr7:6010084-6010134	IMR90	lung:	fetal
45	chr7:6014034-6014084	MCF-7	breast:	n/a
46	chr7:6010084-6010134	AG09319	gingival:	n/a
47	chr7:6014034-6014084	SK-N-SH_RA	brain:	n/a
48	chr7:6014034-6014084	PrEC	prostate:	n/a
49	chr7:6014034-6014084	HRE	kidney:	n/a
50	chr7:6014034-6014084	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
RSPH10B	TF binding region
RSPH10B	CpG island

Extended variants
information (count: 180 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:180 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1180620	chr7:6010086-6010087	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs201109754	chr7:6010118-6010119	Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs529780235	chr7:6010167-6010168	Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541575322	chr7:6010243-6010244	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs62454742	chr7:6010282-6010283	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs62454743	chr7:6010537-6010538	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs111735689	chr7:6010561-6010562	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs1180618	chr7:6011267-6011268	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs377707282	chr7:6011881-6011882	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs370987809	chr7:6011891-6011892	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs374169426	chr7:6011909-6011910	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs111584000	chr7:6011922-6011923	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552864607	chr7:6011939-6011940	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs574825411	chr7:6011993-6011994	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374061444	chr7:6012121-6012122	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs75679751	chr7:6012325-6012326	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs531961545	chr7:6012326-6012327	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs386709792	chr7:6012380-6012381	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs187198918	chr7:6012381-6012382	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374762935	chr7:6012456-6012457	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs570237578	chr7:6012460-6012461	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200687421	chr7:6012469-6012470	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563432331	chr7:6012495-6012496	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1180615	chr7:6012505-6012506	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs530742257	chr7:6012507-6012508	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs192135471	chr7:6012527-6012528	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs568398778	chr7:6012543-6012544	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs183503560	chr7:6012695-6012696	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs62454744	chr7:6012700-6012701	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs1180614	chr7:6012716-6012717	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553849352	chr7:6012772-6012773	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs566288386	chr7:6012823-6012824	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533727628	chr7:6012865-6012866	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs558375877	chr7:6012877-6012878	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs148520351	chr7:6012923-6012924	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs267608145	chr7:6012937-6012938	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs371106085	chr7:6012993-6012994	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs374503068	chr7:6012996-6012997	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs371988762	chr7:6012997-6012998	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs374143144	chr7:6013008-6013009	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556089649	chr7:6013013-6013014	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs368036201	chr7:6013047-6013048	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs1802683	chr7:6013049-6013050	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs574371474	chr7:6013059-6013060	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs371673459	chr7:6013060-6013061	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs267608174	chr7:6013091-6013092	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs10000	chr7:6013153-6013154	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560300531	chr7:6013242-6013243	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs527425812	chr7:6013291-6013292	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs375287353	chr7:6014030-6014031	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6010000-6010200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:6010000-6010200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:6010000-6010200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:6010000-6010200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr7:6010000-6010200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:6010000-6010200	Enhancers	Fetal Muscle Leg	muscle
7	chr7:6010000-6010200	Enhancers	Lung	lung
8	chr7:6010000-6010400	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr7:6010000-6010400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:6010000-6010400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr7:6010000-6010400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr7:6010000-6010400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:6010000-6010400	Active TSS	Fetal Brain Female	brain
14	chr7:6010200-6010400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:6010200-6017200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:6010200-6018400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:6010200-6018600	Weak transcription	Fetal Muscle Leg	muscle
18	chr7:6010200-6021200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:6010200-6026600	Weak transcription	Lung	lung
20	chr7:6010200-6026800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:6010400-6016000	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr7:6010400-6017400	Weak transcription	Fetal Brain Female	brain
23	chr7:6010400-6026200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:6010400-6026600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr7:6010400-6028600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr7:6010400-6048000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:6010600-6018800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:6011200-6017200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:6011400-6026600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr7:6012000-6017600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:6012400-6028800	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr7:6013000-6017600	Weak transcription	Adipose Nuclei	Adipose
33	chr7:6014400-6016000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:6014400-6017200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr7:6014600-6016200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:6014600-6016800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr7:6014600-6027200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:6015000-6017600	Weak transcription	Fetal Intestine Small	intestine
39	chr7:6015000-6026400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr7:6015200-6016800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:6015200-6016800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr7:6015200-6018000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr7:6015200-6026600	Weak transcription	Spleen	Spleen
44	chr7:6015200-6028600	Weak transcription	Gastric	stomach
45	chr7:6015400-6017000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:6015400-6017000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr7:6015400-6017600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:6015400-6023600	Weak transcription	Dnd41	blood
49	chr7:6015600-6017200	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr7:6015600-6017200	Weak transcription	Liver	Liver

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