Variant report

Variant	nsv970565
Chromosome Location	chr7:102781208-102782697
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	CTCF	chr7:102782160-102782310	GM12870	blood:	n/a	n/a
2	CTCF	chr7:102782440-102782590	NHEK	skin:	n/a	n/a
3	EBF1	chr7:102782536-102782729	GM12878	blood:	n/a	n/a
4	EP300	chr7:102782457-102782818	SK-N-SH_RA	brain:	n/a	chr7:102782667-102782676 chr7:102782663-102782677
5	FOS	chr7:102782529-102783341	HUVEC	blood vessel:	n/a	chr7:102783144-102783155
6	FOS	chr7:102782616-102782718	MCF10A-Er-Src	breast:	n/a	n/a
7	IKZF1	chr7:102782530-102782744	GM12878	blood:	n/a	n/a
8	IRF1	chr7:102781301-102781371	K562	blood:	n/a	n/a
9	MAFF	chr7:102781134-102781548	K562	blood:	n/a	chr7:102781321-102781335 chr7:102781322-102781340
10	MAFF	chr7:102781138-102781517	HepG2	liver:	n/a	chr7:102781321-102781335 chr7:102781322-102781340
11	MAFK	chr7:102781150-102781561	HepG2	liver:	n/a	chr7:102781326-102781340 chr7:102781328-102781339 chr7:102781321-102781335 chr7:102781327-102781338 chr7:102781320-102781336 chr7:102781318-102781338 chr7:102781323-102781338 chr7:102781328-102781339 chr7:102781327-102781338
12	MAFK	chr7:102781177-102781654	H1-hESC	embryonic stem cell:	n/a	chr7:102781326-102781340 chr7:102781328-102781339 chr7:102781321-102781335 chr7:102781327-102781338 chr7:102781320-102781336 chr7:102781318-102781338 chr7:102781323-102781338 chr7:102781328-102781339 chr7:102781327-102781338
13	MAFK	chr7:102781140-102781512	IMR90	lung:	n/a	chr7:102781326-102781340 chr7:102781328-102781339 chr7:102781321-102781335 chr7:102781327-102781338 chr7:102781320-102781336 chr7:102781318-102781338 chr7:102781323-102781338 chr7:102781328-102781339 chr7:102781327-102781338
14	MAFK	chr7:102781145-102781537	K562	blood:	n/a	chr7:102781326-102781340 chr7:102781328-102781339 chr7:102781321-102781335 chr7:102781327-102781338 chr7:102781320-102781336 chr7:102781318-102781338 chr7:102781323-102781338 chr7:102781328-102781339 chr7:102781327-102781338
15	MAFK	chr7:102781141-102781516	HepG2	liver:	n/a	chr7:102781326-102781340 chr7:102781328-102781339 chr7:102781321-102781335 chr7:102781327-102781338 chr7:102781320-102781336 chr7:102781318-102781338 chr7:102781323-102781338 chr7:102781328-102781339 chr7:102781327-102781338
16	MAFK	chr7:102781172-102781509	Hela-S3	cervix:	n/a	chr7:102781326-102781340 chr7:102781328-102781339 chr7:102781321-102781335 chr7:102781327-102781338 chr7:102781320-102781336 chr7:102781318-102781338 chr7:102781323-102781338 chr7:102781328-102781339 chr7:102781327-102781338
17	POLR2A	chr7:102781525-102781614	ProgFib	skin:	n/a	n/a
18	POLR2A	chr7:102781994-102782170	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr7:102781550-102781598	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr7:102781490-102781719	HepG2	liver:	n/a	n/a
21	RUNX3	chr7:102782478-102782821	GM12878	blood:	n/a	n/a
22	STAT3	chr7:102782589-102782683	MCF10A-Er-Src	breast:	n/a	n/a
23	TAF1	chr7:102782588-102782772	SK-N-SH	brain:	n/a	n/a
24	TCF12	chr7:102782355-102782887	SK-N-SH	brain:	n/a	n/a
25	TCF7L2	chr7:102782371-102782699	PANC-1	pancreas:	n/a	chr7:102782596-102782605 chr7:102782593-102782607 chr7:102782592-102782608 chr7:102782594-102782604 chr7:102782592-102782608

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102782124-102782174	NHDF-neo	bronchial:	n/a
2	chr7:102782124-102782174	ProgFib	skin:	n/a
3	chr7:102782124-102782174	HCM	heart:	n/a
4	chr7:102782124-102782174	U87	brain:	n/a
5	chr7:102782124-102782174	Caco-2	colon:	n/a
6	chr7:102782124-102782174	HepG2	liver:	n/a
7	chr7:102782124-102782174	HEK293	kidney:	embryo
8	chr7:102782124-102782174	HIPEpiC	eye:	n/a
9	chr7:102782124-102782174	BJ	skin:	n/a
10	chr7:102782124-102782174	CMK	blood:	n/a
11	chr7:102782124-102782174	NH-A	brain:	n/a
12	chr7:102782124-102782174	PrEC	prostate:	n/a
13	chr7:102782124-102782174	RPTEC	kidney:	n/a
14	chr7:102782124-102782174	AG09309	skin:	n/a
15	chr7:102782124-102782174	HNPCEpiC	eye:	n/a
16	chr7:102782124-102782174	GM12891	blood:	n/a
17	chr7:102782124-102782174	SAEC	small airway:	n/a
18	chr7:102782124-102782174	HCT-116	colon:	n/a
19	chr7:102782124-102782174	HRE	kidney:	n/a
20	chr7:102782124-102782174	LNCaP	prostate:	n/a
21	chr7:102782124-102782174	HRCEpiC	kidney:	n/a
22	chr7:102782124-102782174	K562	blood:	n/a
23	chr7:102782124-102782174	T-47D	breast:	n/a
24	chr7:102782124-102782174	H1-hESC	embryonic stem cell:	embryo
25	chr7:102782124-102782174	SK-N-SH	brain:	n/a
26	chr7:102782124-102782174	NT2-D1	testis:	n/a
27	chr7:102782124-102782174	Hepatocyte	liver:	n/a
28	chr7:102782124-102782174	HMEC	breast:	n/a
29	chr7:102782124-102782174	MCF10A-Er-Src	breast:	n/a
30	chr7:102782124-102782174	NB4	blood:	n/a
31	chr7:102782124-102782174	NHBE	bronchial:	n/a
32	chr7:102782124-102782174	AG10803	skin:	n/a
33	chr7:102782124-102782174	GM06990	blood:	n/a
34	chr7:102782124-102782174	AoSMC	blood vessel:	n/a
35	chr7:102782124-102782174	ovcar-3	ovarian:	n/a
36	chr7:102782124-102782174	HCPEpiC	choroid plexus:	n/a
37	chr7:102782124-102782174	MCF-7	breast:	n/a
38	chr7:102782124-102782174	SK-N-SH_RA	brain:	n/a
39	chr7:102782124-102782174	HEEpiC	esophagus:	n/a
40	chr7:102782124-102782174	GM12878	blood:	n/a
41	chr7:102782124-102782174	SK-N-MC	brain:	n/a
42	chr7:102782124-102782174	AG04449	skin:	fetal
43	chr7:102782124-102782174	IMR90	lung:	fetal
44	chr7:102782124-102782174	HL-60	blood:	n/a
45	chr7:102782124-102782174	Hela-S3	cervix:	n/a
46	chr7:102782124-102782174	AG09319	gingival:	n/a
47	chr7:102782124-102782174	A549	lung:	n/a
48	chr7:102782124-102782174	PFSK-1	brain:	n/a
49	chr7:102782124-102782174	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:102782124-102782174	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:102754783..102757571-chr7:102779422..102781825,2	MCF-7	breast:
2	chr7:102779926..102783136-chr7:102788446..102789979,3	MCF-7	breast:
3	chr7:102780818..102786371-chr7:102786977..102791342,10	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXL13-1	chr7:102781717-102782850	NR_026660

Variant related genes	Relation type
RPL19P12	TF binding region
RPL19P12	CpG island
ENSG00000161048	chromatin interactions
CREB5	miRNA target sites

Extended variants
information (count: 64 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:64 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375607945	chr7:102781286-102781287	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553106929	chr7:102781301-102781302	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536391711	chr7:102781373-102781374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs578128236	chr7:102781395-102781396	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs188658694	chr7:102781402-102781403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138292351	chr7:102781415-102781416	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548403824	chr7:102781524-102781525	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs547006109	chr7:102781532-102781533	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569895360	chr7:102781533-102781534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537330024	chr7:102781542-102781543	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191618607	chr7:102781583-102781584	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577479505	chr7:102781605-102781606	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115635296	chr7:102781642-102781643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570326320	chr7:102781643-102781644	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200895189	chr7:102781684-102781685	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs370514767	chr7:102781685-102781686	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145490371	chr7:102781686-102781687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531369016	chr7:102781687-102781688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1140867	chr7:102781714-102781715	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534616317	chr7:102781716-102781717	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185330469	chr7:102781753-102781754	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs574465039	chr7:102781791-102781792	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs376443686	chr7:102781808-102781809	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs535218001	chr7:102781810-102781811	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs554721477	chr7:102781829-102781830	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs112975931	chr7:102781834-102781835	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs543670939	chr7:102781909-102781910	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs71110820	chr7:102781932-102781933	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs140046322	chr7:102781933-102781934	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs147620044	chr7:102781934-102781935	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs565591887	chr7:102781935-102781936	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs577116050	chr7:102781936-102781937	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs190226590	chr7:102781951-102781952	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs559537614	chr7:102782032-102782033	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs530197716	chr7:102782035-102782036	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs7795941	chr7:102782050-102782051	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370475617	chr7:102782062-102782063	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs181476817	chr7:102782067-102782068	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs530748902	chr7:102782076-102782077	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs552453373	chr7:102782105-102782106	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs563224006	chr7:102782106-102782107	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs146496282	chr7:102782110-102782111	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs111278816	chr7:102782113-102782114	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs112038401	chr7:102782125-102782126	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs187425287	chr7:102782130-102782131	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs542253565	chr7:102782135-102782136	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs567990320	chr7:102782176-102782177	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs535163423	chr7:102782196-102782197	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs556653484	chr7:102782232-102782233	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs189325083	chr7:102782246-102782247	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21510904	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102747400-102781800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:102747600-102789200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:102760600-102782000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:102760600-102782200	Weak transcription	HSMM	muscle
5	chr7:102764000-102781800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:102764200-102787000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:102767200-102786000	Weak transcription	GM12878-XiMat	blood
8	chr7:102768800-102781800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:102768800-102782000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:102768800-102782000	Weak transcription	Pancreas	Pancrea
11	chr7:102768800-102786000	Weak transcription	Brain Germinal Matrix	brain
12	chr7:102768800-102786200	Weak transcription	Fetal Heart	heart
13	chr7:102768800-102786600	Weak transcription	Lung	lung
14	chr7:102768800-102788600	Weak transcription	Right Ventricle	heart
15	chr7:102769000-102781400	Weak transcription	Dnd41	blood
16	chr7:102769000-102782000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:102769000-102786000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:102769000-102786000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:102769000-102786000	Weak transcription	Fetal Brain Male	brain
20	chr7:102769000-102786600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:102769000-102786800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:102769000-102787000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr7:102769200-102781800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:102769200-102781800	Weak transcription	Fetal Muscle Trunk	muscle
25	chr7:102769200-102781800	Weak transcription	Fetal Thymus	thymus
26	chr7:102769200-102786000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr7:102769200-102786600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:102769200-102786800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:102769200-102787000	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr7:102769200-102787000	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr7:102769200-102787000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr7:102769200-102787200	Weak transcription	Adipose Nuclei	Adipose
33	chr7:102769200-102787800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr7:102769200-102788200	Weak transcription	Primary B cells from cord blood	blood
35	chr7:102769200-102788400	Weak transcription	Thymus	Thymus
36	chr7:102770800-102781800	Weak transcription	Primary T cells from cord blood	blood
37	chr7:102771000-102786600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:102771000-102788800	Weak transcription	Small Intestine	intestine
39	chr7:102771200-102783000	Weak transcription	A549	lung
40	chr7:102771600-102784000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr7:102772600-102781800	Weak transcription	Fetal Intestine Small	intestine
42	chr7:102772600-102781800	Weak transcription	Fetal Stomach	stomach
43	chr7:102774000-102782000	Weak transcription	Fetal Muscle Leg	muscle
44	chr7:102774000-102782600	Weak transcription	Spleen	Spleen
45	chr7:102774000-102783800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr7:102774000-102788600	Weak transcription	HSMMtube	muscle
47	chr7:102774200-102784200	Weak transcription	HepG2	liver
48	chr7:102774200-102786000	Weak transcription	Liver	Liver
49	chr7:102774200-102786400	Weak transcription	Aorta	Aorta
50	chr7:102774200-102786600	Weak transcription	Left Ventricle	heart

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