Variant report

Variant	nsv1023476
Chromosome Location	chr7:102238120-102357753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3307)
CpG islands
(count:977)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3307 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
2	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
3	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
4	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
5	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
6	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
7	BATF	chr7:102254118-102255225	GM12878	blood:	n/a	n/a
8	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
9	BATF	chr7:102266316-102266513	GM12878	blood:	n/a	n/a
10	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
11	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
12	BATF	chr7:102256202-102256653	GM12878	blood:	n/a	n/a
13	BATF	chr7:102254763-102255038	GM12878	blood:	n/a	n/a
14	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
15	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
16	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
17	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
18	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
19	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
20	BATF	chr7:102353721-102354553	GM12878	blood:	n/a	n/a
21	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
22	BATF	chr7:102257362-102257620	GM12878	blood:	n/a	n/a
23	BATF	chr7:102251367-102251812	GM12878	blood:	n/a	n/a
24	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
25	BATF	chr7:102247244-102247556	GM12878	blood:	n/a	n/a
26	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
27	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
28	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
29	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
30	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
31	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
32	BATF	chr7:102356109-102356632	GM12878	blood:	n/a	n/a
33	BATF	chr7:102252871-102253062	GM12878	blood:	n/a	n/a
34	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
35	BATF	chr7:102355431-102355796	GM12878	blood:	n/a	n/a
36	BATF	chr7:102352630-102352884	GM12878	blood:	n/a	n/a
37	BATF	chr7:102254253-102254722	GM12878	blood:	n/a	n/a
38	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
39	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
40	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
41	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
42	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:102310787-102310962	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102277264-102277434	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:102353630-102354526	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:102255171-102255360	GM12878	blood:	n/a	chr7:102255318-102255331
47	BCL11A	chr7:102354099-102354536	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:102306449-102306783	GM12878	blood:	n/a	n/a
49	BCL11A	chr7:102256423-102256656	GM12878	blood:	n/a	n/a
50	BCL11A	chr7:102330097-102330855	GM12878	blood:	n/a	chr7:102330751-102330764

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102312315-102312365	SK-N-MC	brain:	n/a
2	chr7:102312315-102312365	SK-N-MC	brain:	n/a
3	chr7:102332458-102332508	SKMC	muscle:	n/a
4	chr7:102311965-102312015	SK-N-SH	brain:	n/a
5	chr7:102327236-102327286	RPTEC	kidney:	n/a
6	chr7:102329146-102329196	HIPEpiC	eye:	n/a
7	chr7:102332458-102332508	PrEC	prostate:	n/a
8	chr7:102259241-102259291	HRCEpiC	kidney:	n/a
9	chr7:102312315-102312365	MCF-7	breast:	n/a
10	chr7:102311965-102312015	SK-N-SH_RA	brain:	n/a
11	chr7:102308061-102308111	RPTEC	kidney:	n/a
12	chr7:102330635-102330685	NHDF-neo	bronchial:	n/a
13	chr7:102330635-102330685	GM12891	blood:	n/a
14	chr7:102332458-102332508	Caco-2	colon:	n/a
15	chr7:102259241-102259291	PFSK-1	brain:	n/a
16	chr7:102327236-102327286	IMR90	lung:	fetal
17	chr7:102312331-102312381	BJ	skin:	n/a
18	chr7:102312308-102312358	PrEC	prostate:	n/a
19	chr7:102330635-102330685	MCF10A-Er-Src	breast:	n/a
20	chr7:102279588-102279638	PANC-1	pancreas:	n/a
21	chr7:102311965-102312015	HMEC	breast:	n/a
22	chr7:102246378-102246428	HRPEpiC	eye:	n/a
23	chr7:102327236-102327286	HRPEpiC	eye:	n/a
24	chr7:102311965-102312015	U87	brain:	n/a
25	chr7:102312331-102312381	Caco-2	colon:	n/a
26	chr7:102312318-102312368	SK-N-SH	brain:	n/a
27	chr7:102311965-102312015	AG04449	skin:	fetal
28	chr7:102312331-102312381	NHBE	bronchial:	n/a
29	chr7:102329146-102329196	AG04449	skin:	fetal
30	chr7:102246378-102246428	HRE	kidney:	n/a
31	chr7:102308061-102308111	BE2_C	brain:	n/a
32	chr7:102312308-102312358	A549	lung:	n/a
33	chr7:102279588-102279638	Jurkat	blood:	n/a
34	chr7:102259241-102259291	ProgFib	skin:	n/a
35	chr7:102312318-102312368	HNPCEpiC	eye:	n/a
36	chr7:102312200-102312250	HNPCEpiC	eye:	n/a
37	chr7:102311965-102312015	NHBE	bronchial:	n/a
38	chr7:102308061-102308111	GM12891	blood:	n/a
39	chr7:102311965-102312015	K562	blood:	n/a
40	chr7:102308061-102308111	HRCEpiC	kidney:	n/a
41	chr7:102312315-102312365	AoSMC	blood vessel:	n/a
42	chr7:102312200-102312250	MCF10A-Er-Src	breast:	n/a
43	chr7:102312331-102312381	HEEpiC	esophagus:	n/a
44	chr7:102312318-102312368	BE2_C	brain:	n/a
45	chr7:102312331-102312381	IMR90	lung:	fetal
46	chr7:102311965-102312015	HCPEpiC	choroid plexus:	n/a
47	chr7:102259241-102259291	BE2_C	brain:	n/a
48	chr7:102259241-102259291	NT2-D1	testis:	n/a
49	chr7:102312315-102312365	HRPEpiC	eye:	n/a
50	chr7:102279588-102279638	HEK293	kidney:	embryo

No data

Variant related genes	Relation type
ENSG00000205236	TF binding region
ENSG00000228049	TF binding region
ENSG00000238997	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
RASA4	TF binding region
RASA4DP	TF binding region
SPDYE2B	TF binding region
ENSG00000205236	CpG island
ENSG00000228049	CpG island
ENSG00000238997	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
RASA4	CpG island
RASA4DP	CpG island
SPDYE2B	CpG island

Extended variants
information (count: 1448 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1448 , 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	rs372491307	chr7:102238131-102238132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574854356	chr7:102238159-102238160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539519998	chr7:102238166-102238167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371599697	chr7:102238369-102238370	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs535516012	chr7:102238372-102238373	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs557287011	chr7:102238434-102238435	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs375271161	chr7:102238589-102238590	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs56189890	chr7:102238693-102238694	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs7781693	chr7:102238697-102238698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7781699	chr7:102238704-102238705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7781311	chr7:102238743-102238744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575869285	chr7:102238760-102238761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561434146	chr7:102238808-102238809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376532262	chr7:102238809-102238810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546049232	chr7:102239802-102239803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373066080	chr7:102239811-102239812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs28663375	chr7:102239854-102239855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs28496872	chr7:102239880-102239881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558021651	chr7:102240111-102240112	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375943301	chr7:102240124-102240125	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs573147986	chr7:102240293-102240294	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370047247	chr7:102240301-102240302	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs148994026	chr7:102240718-102240719	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs112083455	chr7:102241619-102241620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146519099	chr7:102241694-102241695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113495281	chr7:102241904-102241905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199760346	chr7:102241995-102241996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139425921	chr7:102242037-102242038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201686518	chr7:102242104-102242105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150058264	chr7:102242190-102242191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369576682	chr7:102242287-102242288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377300132	chr7:102242298-102242299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113905264	chr7:102243415-102243416	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs112457023	chr7:102243416-102243417	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs112003076	chr7:102243688-102243689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370234047	chr7:102243721-102243722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145217665	chr7:102243787-102243788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9656077	chr7:102243799-102243800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561668373	chr7:102243952-102243953	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs372714791	chr7:102244067-102244068	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs374863036	chr7:102244124-102244125	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs528951049	chr7:102244145-102244146	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375942804	chr7:102244231-102244232	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs543888847	chr7:102244246-102244247	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs148681177	chr7:102244286-102244287	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs572836856	chr7:102244302-102244303	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs202035657	chr7:102244303-102244304	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375917275	chr7:102244310-102244311	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537044454	chr7:102244324-102244325	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs59719405	chr7:102244385-102244386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102236200-102252400	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:102242200-102242400	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr7:102242400-102246000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr7:102242600-102252400	Weak transcription	Ovary	ovary
5	chr7:102244000-102244200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:102244000-102244200	Enhancers	Placenta Amnion	Placenta Amnion
7	chr7:102244000-102244200	Enhancers	K562	blood
8	chr7:102244000-102244400	Enhancers	Hela-S3	cervix
9	chr7:102244200-102244400	Enhancers	Stomach Smooth Muscle	stomach
10	chr7:102244200-102252400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:102244200-102252400	Weak transcription	Lung	lung
12	chr7:102244200-102252400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr7:102244400-102246000	Weak transcription	Hela-S3	cervix
14	chr7:102244800-102252400	Weak transcription	Fetal Stomach	stomach
15	chr7:102245200-102252400	Weak transcription	Fetal Brain Female	brain
16	chr7:102246000-102246200	Enhancers	Hela-S3	cervix
17	chr7:102246000-102246400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:102246000-102246800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr7:102246000-102246800	Enhancers	K562	blood
20	chr7:102246000-102252400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr7:102246400-102246800	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr7:102246400-102252200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr7:102246400-102252400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:102246800-102251000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:102246800-102252400	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr7:102246800-102252400	Weak transcription	K562	blood
27	chr7:102251000-102251200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:102251000-102251200	Enhancers	Primary B cells from peripheral blood	blood
29	chr7:102251000-102251200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr7:102251000-102251200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:102251000-102251200	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr7:102251000-102251200	Enhancers	A549	lung
33	chr7:102251000-102251200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr7:102251200-102252200	Weak transcription	A549	lung
35	chr7:102251200-102252200	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr7:102251200-102252400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:102251200-102252400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:102251200-102252400	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr7:102251400-102252400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr7:102251400-102252400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr7:102252200-102252400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:102252200-102252400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr7:102252200-102252400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr7:102252200-102252400	Enhancers	Adipose Nuclei	Adipose
45	chr7:102252200-102252400	Enhancers	Brain Anterior Caudate	brain
46	chr7:102252200-102252400	Enhancers	Rectal Smooth Muscle	rectum
47	chr7:102252200-102252400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr7:102252200-102252400	Enhancers	Stomach Smooth Muscle	stomach
49	chr7:102252200-102252400	Enhancers	Dnd41	blood
50	chr7:102252200-102252400	Enhancers	GM12878-XiMat	blood

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