Variant report

Variant	nsv971390
Chromosome Location	chr7:65441078-65445874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:65445769-65446159	K562	blood:	n/a	n/a
2	ATF2	chr7:65445705-65446301	GM12878	blood:	n/a	n/a
3	ATF2	chr7:65445713-65446255	GM12878	blood:	n/a	n/a
4	BCL11A	chr7:65445804-65446185	GM12878	blood:	n/a	n/a
5	BCLAF1	chr7:65445700-65446344	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:65445579-65446242	K562	blood:	n/a	n/a
7	BHLHE40	chr7:65445743-65446248	GM12878	blood:	n/a	n/a
8	CBX3	chr7:65445617-65446294	K562	blood:	n/a	n/a
9	CCNT2	chr7:65445729-65446235	K562	blood:	n/a	n/a
10	CEBPB	chr7:65442107-65442335	K562	blood:	n/a	n/a
11	CEBPB	chr7:65445614-65446288	GM12878	blood:	n/a	n/a
12	CHD1	chr7:65445638-65446195	GM12878	blood:	n/a	n/a
13	CHD2	chr7:65445752-65446128	GM12878	blood:	n/a	n/a
14	CREB1	chr7:65445614-65446332	GM12878	blood:	n/a	n/a
15	CTCF	chr7:65440940-65441090	RPTEC	kidney:	n/a	n/a
16	CTCF	chr7:65440857-65441108	HepG2	liver:	n/a	n/a
17	CTCF	chr7:65440940-65441090	GM12872	blood:	n/a	n/a
18	CTCF	chr7:65440905-65441108	K562	blood:	n/a	n/a
19	EBF1	chr7:65445857-65446211	GM12878	blood:	n/a	n/a
20	EBF1	chr7:65445816-65446118	GM12878	blood:	n/a	n/a
21	EGR1	chr7:65445824-65446320	K562	blood:	n/a	chr7:65446083-65446097
22	EGR1	chr7:65445865-65446317	MCF-7	breast:	n/a	chr7:65446083-65446097
23	EGR1	chr7:65445865-65446277	K562	blood:	n/a	chr7:65446083-65446097
24	ELF1	chr7:65445531-65446171	K562	blood:	n/a	chr7:65446041-65446053
25	ELF1	chr7:65445712-65446228	GM12878	blood:	n/a	chr7:65446041-65446053
26	ELF1	chr7:65445707-65446207	MCF-7	breast:	n/a	chr7:65446041-65446053
27	ELF1	chr7:65445702-65446189	K562	blood:	n/a	chr7:65446041-65446053
28	ELK1	chr7:65445839-65445865	K562	blood:	n/a	n/a
29	EP300	chr7:65445597-65446064	GM12878	blood:	n/a	n/a
30	EP300	chr7:65445794-65446348	K562	blood:	n/a	n/a
31	EP300	chr7:65445793-65446157	GM12878	blood:	n/a	n/a
32	FOXM1	chr7:65445666-65446301	GM12878	blood:	n/a	n/a
33	GABPA	chr7:65445778-65446085	GM12878	blood:	n/a	n/a
34	GABPA	chr7:65445798-65446154	K562	blood:	n/a	n/a
35	GABPA	chr7:65445574-65446270	K562	blood:	n/a	n/a
36	GABPA	chr7:65445704-65446199	MCF-7	breast:	n/a	n/a
37	HCFC1	chr7:65445731-65446187	K562	blood:	n/a	n/a
38	HDAC2	chr7:65445855-65446192	K562	blood:	n/a	n/a
39	HEY1	chr7:65445825-65446170	K562	blood:	n/a	n/a
40	HEY1	chr7:65443697-65444022	K562	blood:	n/a	n/a
41	HEY1	chr7:65445110-65446531	K562	blood:	n/a	n/a
42	HEY1	chr7:65444228-65445098	K562	blood:	n/a	n/a
43	IRF1	chr7:65445857-65446127	K562	blood:	n/a	n/a
44	IRF4	chr7:65445829-65446186	GM12878	blood:	n/a	n/a
45	IRF4	chr7:65445847-65446244	GM12878	blood:	n/a	n/a
46	JUND	chr7:65444292-65444579	HepG2	liver:	n/a	n/a
47	JUND	chr7:65445758-65446200	K562	blood:	n/a	n/a
48	MAX	chr7:65445519-65446277	K562	blood:	n/a	n/a
49	MAX	chr7:65445598-65446242	GM12878	blood:	n/a	n/a
50	MAX	chr7:65440921-65441088	NB4	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65445384-65445434	Hela-S3	cervix:	n/a
2	chr7:65445384-65445434	A549	lung:	n/a
3	chr7:65445384-65445434	T-47D	breast:	n/a
4	chr7:65444356-65444406	Hela-S3	cervix:	n/a
5	chr7:65444356-65444406	HRPEpiC	eye:	n/a
6	chr7:65445384-65445434	GM06990	blood:	n/a
7	chr7:65444356-65444406	NHDF-neo	bronchial:	n/a
8	chr7:65444356-65444406	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:65445384-65445434	HIPEpiC	eye:	n/a
10	chr7:65444356-65444406	NT2-D1	testis:	n/a
11	chr7:65445384-65445434	HL-60	blood:	n/a
12	chr7:65445384-65445434	Caco-2	colon:	n/a
13	chr7:65445384-65445434	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:65445384-65445434	GM12891	blood:	n/a
15	chr7:65445384-65445434	HCPEpiC	choroid plexus:	n/a
16	chr7:65445384-65445434	SK-N-SH	brain:	n/a
17	chr7:65445384-65445434	NH-A	brain:	n/a
18	chr7:65445384-65445434	HCF	heart:	n/a
19	chr7:65445384-65445434	ECC-1	luminal epithelium:	n/a
20	chr7:65445384-65445434	AG09319	gingival:	n/a
21	chr7:65445384-65445434	GM12892	blood:	n/a
22	chr7:65445384-65445434	AG04450	lung:	fetal
23	chr7:65444356-65444406	BE2_C	brain:	n/a
24	chr7:65445384-65445434	NHDF-neo	bronchial:	n/a
25	chr7:65445384-65445434	HEK293	kidney:	embryo
26	chr7:65444356-65444406	GM06990	blood:	n/a
27	chr7:65444356-65444406	HUVEC	blood vessel:	n/a
28	chr7:65445384-65445434	SAEC	small airway:	n/a
29	chr7:65444356-65444406	HL-60	blood:	n/a
30	chr7:65444356-65444406	CMK	blood:	n/a
31	chr7:65444356-65444406	PrEC	prostate:	n/a
32	chr7:65444356-65444406	AG04450	lung:	fetal
33	chr7:65444356-65444406	U87	brain:	n/a
34	chr7:65444356-65444406	H1-hESC	embryonic stem cell:	embryo
35	chr7:65445384-65445434	IMR90	lung:	fetal
36	chr7:65444356-65444406	HMEC	breast:	n/a
37	chr7:65445384-65445434	HRE	kidney:	n/a
38	chr7:65445384-65445434	HEEpiC	esophagus:	n/a
39	chr7:65444356-65444406	ovcar-3	ovarian:	n/a
40	chr7:65444356-65444406	NB4	blood:	n/a
41	chr7:65445384-65445434	HUVEC	blood vessel:	n/a
42	chr7:65445384-65445434	BE2_C	brain:	n/a
43	chr7:65444356-65444406	ProgFib	skin:	n/a
44	chr7:65445384-65445434	U87	brain:	n/a
45	chr7:65445384-65445434	HMEC	breast:	n/a
46	chr7:65445384-65445434	BJ	skin:	n/a
47	chr7:65444356-65444406	SK-N-SH_RA	brain:	n/a
48	chr7:65444356-65444406	GM19239	blood:	n/a
49	chr7:65444356-65444406	ECC-1	luminal epithelium:	n/a
50	chr7:65444356-65444406	Caco-2	colon:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65441240..65443607-chr7:65444690..65447035,2	MCF-7	breast:
2	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
3	chr7:65439784..65442429-chr7:65442521..65444614,2	MCF-7	breast:
4	chr7:65439784..65442429-chr7:65442521..65444614,2	MCF-7	breast:
5	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
6	chr7:65445709..65448649-chr7:65579782..65581390,2	K562	blood:
7	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
8	chr7:65439470..65441298-chr7:65540371..65542201,2	K562	blood:
9	chr7:65431361..65432924-chr7:65439699..65441509,2	K562	blood:
10	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:

No data

Variant related genes	Relation type
GUSB	TF binding region
GUSB	CpG island
ENSG00000126522	chromatin interactions
ENSG00000169919	chromatin interactions
ENSG00000196715	chromatin interactions
ENSG00000241258	chromatin interactions

Extended variants
information (count: 242 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:242 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150999162	chr7:65441101-65441102	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs369465888	chr7:65441102-65441103	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs571704452	chr7:65441107-65441108	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373590814	chr7:65441132-65441133	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200941434	chr7:65441148-65441149	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs140709901	chr7:65441150-65441151	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs150086524	chr7:65441154-65441155	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs62470936	chr7:65441205-65441206	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs371485895	chr7:65441206-65441207	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs376639818	chr7:65441230-65441231	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs571815706	chr7:65441247-65441248	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs191138389	chr7:65441303-65441304	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557530842	chr7:65441309-65441310	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs367942939	chr7:65441315-65441316	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs574079516	chr7:65441318-65441319	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543078465	chr7:65441321-65441322	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs78667474	chr7:65441330-65441331	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs74881155	chr7:65441331-65441332	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529825087	chr7:65441335-65441336	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs75767674	chr7:65441356-65441357	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs4451200	chr7:65441370-65441371	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572217782	chr7:65441381-65441382	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550592075	chr7:65441393-65441394	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184769896	chr7:65441403-65441404	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532998108	chr7:65441431-65441432	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543107743	chr7:65441440-65441441	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371866379	chr7:65441476-65441477	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs190435442	chr7:65441523-65441524	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs181764572	chr7:65441542-65441543	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs529892226	chr7:65441545-65441546	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548670348	chr7:65441601-65441602	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565693556	chr7:65441602-65441603	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs528735116	chr7:65441608-65441609	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552061468	chr7:65441611-65441612	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs185256227	chr7:65441700-65441701	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189789123	chr7:65441713-65441714	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551072712	chr7:65441716-65441717	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35248213	chr7:65441730-65441731	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144103641	chr7:65441747-65441748	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73150003	chr7:65441791-65441792	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536764936	chr7:65441794-65441795	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376515212	chr7:65441805-65441806	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs369490956	chr7:65441806-65441807	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373710660	chr7:65441830-65441831	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534602045	chr7:65441917-65441918	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs181191584	chr7:65441938-65441939	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140310412	chr7:65441948-65441949	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs543250631	chr7:65441957-65441958	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563920867	chr7:65441959-65441960	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs144170020	chr7:65441964-65441965	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Glioblastoma	21080181	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Chronic myeloid leukemia	18641042	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65417800-65441600	Strong transcription	Primary T cells from cord blood	blood
2	chr7:65417800-65445400	Weak transcription	Fetal Heart	heart
3	chr7:65418000-65445400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr7:65418400-65442400	Strong transcription	Adipose Nuclei	Adipose
5	chr7:65418400-65445200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:65418800-65442400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr7:65418800-65444000	Strong transcription	Dnd41	blood
8	chr7:65418800-65445200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:65418800-65445400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:65418800-65445600	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:65418800-65446000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:65419000-65442400	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:65419000-65442400	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr7:65419000-65442600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr7:65419000-65445200	Strong transcription	Fetal Muscle Trunk	muscle
16	chr7:65419000-65445400	Strong transcription	Fetal Thymus	thymus
17	chr7:65419000-65445400	Strong transcription	Thymus	Thymus
18	chr7:65419200-65445200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:65419400-65445200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr7:65419600-65442400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:65419600-65444800	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr7:65419800-65445400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:65420200-65445200	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:65420400-65442200	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr7:65420600-65442400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:65420600-65442400	Strong transcription	Fetal Brain Female	brain
27	chr7:65422400-65444800	Strong transcription	Brain Germinal Matrix	brain
28	chr7:65422400-65445600	Weak transcription	Right Atrium	heart
29	chr7:65422600-65442400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:65423000-65441200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr7:65423000-65441200	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr7:65423000-65442400	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr7:65423000-65442400	Strong transcription	Stomach Smooth Muscle	stomach
34	chr7:65423000-65444800	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr7:65423000-65445600	Strong transcription	Fetal Intestine Large	intestine
36	chr7:65423200-65442400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:65423400-65442200	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr7:65423400-65442400	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr7:65423600-65442200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr7:65423600-65442400	Strong transcription	Right Ventricle	heart
41	chr7:65423600-65445000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr7:65423600-65445400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:65423600-65445400	Strong transcription	Fetal Muscle Leg	muscle
44	chr7:65423800-65441200	Strong transcription	Aorta	Aorta
45	chr7:65423800-65442400	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr7:65423800-65442400	Strong transcription	Left Ventricle	heart
47	chr7:65423800-65445400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:65424000-65442400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr7:65424000-65444400	Strong transcription	Fetal Stomach	stomach
50	chr7:65424000-65445400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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