Variant report

Variant	esv1796336
Chromosome Location	chr10:112848721-112878724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 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	BHLHE40	chr10:112858646-112858648	K562	blood:	n/a	n/a
2	CEBPB	chr10:112866822-112866833	HepG2	liver:	n/a	n/a
3	CTCF	chr10:112866900-112867050	RPTEC	kidney:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
4	CTCF	chr10:112858643-112858670	HUVEC	blood vessel:	n/a	n/a
5	CTCF	chr10:112858580-112858730	GM12869	blood:	n/a	n/a
6	CTCF	chr10:112866906-112867002	HepG2	liver:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
7	CTCF	chr10:112866800-112866950	HCT-116	colon:	n/a	n/a
8	CTCF	chr10:112858620-112858770	SAEC	small airway:	n/a	n/a
9	CTCF	chr10:112866840-112866990	HEK293	kidney:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
10	CTCF	chr10:112858520-112858670	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr10:112858573-112858759	GM19240	blood:	n/a	n/a
12	CTCF	chr10:112858574-112858764	K562	blood:	n/a	n/a
13	CTCF	chr10:112858600-112858750	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr10:112858410-112858891	HCT-116	colon:	n/a	chr10:112858808-112858826
15	CTCF	chr10:112858605-112858738	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr10:112858540-112858690	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr10:112866937-112866943	GM10248	blood:	n/a	n/a
18	CTCF	chr10:112866900-112867050	A549	lung:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
19	CTCF	chr10:112858480-112858630	GM12870	blood:	n/a	n/a
20	CTCF	chr10:112858560-112858710	GM12874	blood:	n/a	n/a
21	CTCF	chr10:112858600-112858750	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr10:112858620-112858770	GM12864	blood:	n/a	n/a
23	CTCF	chr10:112858580-112858730	GM12874	blood:	n/a	n/a
24	CTCF	chr10:112858570-112858769	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:112858600-112858750	HMF	breast:	n/a	n/a
26	CTCF	chr10:112858620-112858770	HVMF	connective:	n/a	n/a
27	CTCF	chr10:112872740-112873010	GM12869	blood:	n/a	n/a
28	CTCF	chr10:112858560-112858710	A549	lung:	n/a	n/a
29	CTCF	chr10:112858720-112858870	A549	lung:	n/a	chr10:112858808-112858826
30	CTCF	chr10:112858640-112858790	GM12864	blood:	n/a	n/a
31	CTCF	chr10:112858674-112858685	NHEK	skin:	n/a	n/a
32	CTCF	chr10:112866833-112867223	K562	blood:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
33	CTCF	chr10:112866940-112867090	HEK293	kidney:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
34	CTCF	chr10:112866840-112866990	Caco-2	colon:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
35	CTCF	chr10:112858507-112858796	K562	blood:	n/a	n/a
36	CTCF	chr10:112858600-112858750	AG09319	gingival:	n/a	n/a
37	CTCF	chr10:112858580-112858730	GM12865	blood:	n/a	n/a
38	CTCF	chr10:112858600-112858750	AG04449	skin:	n/a	n/a
39	CTCF	chr10:112858648-112858673	Lung_OC	lung:	n/a	n/a
40	CTCF	chr10:112866754-112867099	H1-hESC	embryonic stem cell:	n/a	chr10:112866789-112866802 chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
41	CTCF	chr10:112858560-112858710	GM12865	blood:	n/a	n/a
42	CTCF	chr10:112858565-112858739	GM12878	blood:	n/a	n/a
43	CTCF	chr10:112858620-112858770	HMEC	breast:	n/a	n/a
44	CTCF	chr10:112858604-112858758	GM19239	blood:	n/a	n/a
45	CTCF	chr10:112866865-112867037	K562	blood:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
46	CTCF	chr10:112858580-112858730	GM12878	blood:	n/a	n/a
47	CTCF	chr10:112858638-112858686	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr10:112866860-112867010	GM12874	blood:	n/a	chr10:112866949-112866958 chr10:112866946-112866964 chr10:112866949-112866962
49	CTCF	chr10:112858572-112858758	Gliobla	brain:	n/a	n/a
50	CTCF	chr10:112858650-112858732	Pancreas_OC	pancreas:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:112867846-112867896	Hepatocyte	liver:	n/a
2	chr10:112864820-112864870	Hepatocyte	liver:	n/a
3	chr10:112867846-112867896	AG04450	lung:	fetal
4	chr10:112867846-112867896	BJ	skin:	n/a
5	chr10:112867846-112867896	Hela-S3	cervix:	n/a
6	chr10:112867846-112867896	HEK293	kidney:	embryo
7	chr10:112864698-112864748	HCT-116	colon:	n/a
8	chr10:112864820-112864870	HEK293	kidney:	embryo
9	chr10:112864820-112864870	BE2_C	brain:	n/a
10	chr10:112864698-112864748	AG04450	lung:	fetal
11	chr10:112864820-112864870	HRPEpiC	eye:	n/a
12	chr10:112864698-112864748	SAEC	small airway:	n/a
13	chr10:112867846-112867896	SAEC	small airway:	n/a
14	chr10:112867846-112867896	MCF10A-Er-Src	breast:	n/a
15	chr10:112864698-112864748	ProgFib	skin:	n/a
16	chr10:112864820-112864870	Caco-2	colon:	n/a
17	chr10:112864820-112864870	MCF10A-Er-Src	breast:	n/a
18	chr10:112864698-112864748	NHDF-neo	bronchial:	n/a
19	chr10:112864698-112864748	ovcar-3	ovarian:	n/a
20	chr10:112864698-112864748	ECC-1	luminal epithelium:	n/a
21	chr10:112864698-112864748	MCF10A-Er-Src	breast:	n/a
22	chr10:112864820-112864870	MCF-7	breast:	n/a
23	chr10:112864698-112864748	HRPEpiC	eye:	n/a
24	chr10:112867846-112867896	PFSK-1	brain:	n/a
25	chr10:112864698-112864748	HRE	kidney:	n/a
26	chr10:112864820-112864870	A549	lung:	n/a
27	chr10:112867846-112867896	HEEpiC	esophagus:	n/a
28	chr10:112864820-112864870	HEEpiC	esophagus:	n/a
29	chr10:112864820-112864870	HAEpiC	amniotic membrane:	n/a
30	chr10:112867846-112867896	RPTEC	kidney:	n/a
31	chr10:112864698-112864748	H1-hESC	embryonic stem cell:	embryo
32	chr10:112864698-112864748	AoSMC	blood vessel:	n/a
33	chr10:112864820-112864870	HCT-116	colon:	n/a
34	chr10:112867846-112867896	Caco-2	colon:	n/a
35	chr10:112864820-112864870	NHDF-neo	bronchial:	n/a
36	chr10:112864698-112864748	GM19239	blood:	n/a
37	chr10:112867846-112867896	LNCaP	prostate:	n/a
38	chr10:112864820-112864870	PrEC	prostate:	n/a
39	chr10:112864820-112864870	GM12891	blood:	n/a
40	chr10:112864820-112864870	GM06990	blood:	n/a
41	chr10:112867846-112867896	HRCEpiC	kidney:	n/a
42	chr10:112864820-112864870	NB4	blood:	n/a
43	chr10:112864698-112864748	Jurkat	blood:	n/a
44	chr10:112867846-112867896	HAEpiC	amniotic membrane:	n/a
45	chr10:112864698-112864748	K562	blood:	n/a
46	chr10:112867846-112867896	IMR90	lung:	fetal
47	chr10:112867846-112867896	HUVEC	blood vessel:	n/a
48	chr10:112864820-112864870	T-47D	breast:	n/a
49	chr10:112864820-112864870	GM19239	blood:	n/a
50	chr10:112864820-112864870	SAEC	small airway:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:112858644..112861642-chr10:112871139..112872875,2	MCF-7	breast:
2	chr10:112677000..112679422-chr10:112861364..112862923,2	MCF-7	breast:
3	chr10:112854536..112855207-chr10:112867276..112868184,2	MCF-7	breast:
4	chr10:112835558..112836069-chr10:112858564..112859533,2	MCF-7	breast:
5	chr10:112854536..112855207-chr10:112867276..112868184,2	MCF-7	breast:
6	chr10:112857274..112860234-chr10:112900319..112903397,3	K562	blood:
7	chr10:112867287..112868074-chr10:113150093..113150654,2	MCF-7	breast:
8	chr10:112858644..112861642-chr10:112871139..112872875,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADRA2A-1	chr10:112877718-112877848	XLOC_008615
2	lnc-ADRA2A-1	chr10:112874075-112874174	XLOC_008615
3	lnc-ADRA2A-3	chr10:112864714-112865006	NONHSAT016385

No data

Variant related genes	Relation type
ENSG00000213247	TF binding region
ENSG00000213247	CpG island
ENSG00000214413	chromatin interactions
ENSG00000108061	chromatin interactions

Extended variants
information (count: 1209 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189105087	chr10:112848721-112848722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78070232	chr10:112848724-112848725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573409895	chr10:112848782-112848783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540764186	chr10:112848829-112848830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148734219	chr10:112848886-112848887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192670542	chr10:112848911-112848912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541782252	chr10:112848918-112848919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142356642	chr10:112848938-112848939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530812937	chr10:112848954-112848955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529886049	chr10:112848956-112848957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150812575	chr10:112849029-112849030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564270259	chr10:112849092-112849093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139279740	chr10:112849157-112849158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144499261	chr10:112849163-112849164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568494460	chr10:112849198-112849199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146645997	chr10:112849226-112849227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111620172	chr10:112849267-112849268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115897258	chr10:112849291-112849292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184699707	chr10:112849300-112849301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141338537	chr10:112849370-112849371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60285632	chr10:112849372-112849373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs564147422	chr10:112849377-112849378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554822050	chr10:112849383-112849384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371477131	chr10:112849396-112849397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145822100	chr10:112849424-112849425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574442064	chr10:112849428-112849429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369548519	chr10:112849437-112849438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541983091	chr10:112849438-112849439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563253175	chr10:112849445-112849446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528427066	chr10:112849454-112849455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60227073	chr10:112849460-112849461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs546111351	chr10:112849478-112849479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568652121	chr10:112849584-112849585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143102882	chr10:112849601-112849602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528377198	chr10:112849602-112849603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540393748	chr10:112849633-112849634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs57258802	chr10:112849638-112849639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529372614	chr10:112849649-112849650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12259584	chr10:112849717-112849718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs188953553	chr10:112849736-112849737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533193019	chr10:112849739-112849740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372981412	chr10:112849789-112849790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570314434	chr10:112849843-112849844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181397407	chr10:112849874-112849875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534618170	chr10:112849882-112849883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567127228	chr10:112849908-112849909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148191057	chr10:112849921-112849922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555915355	chr10:112849932-112849933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567794089	chr10:112849962-112849963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535541679	chr10:112849979-112849980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112839400-112848800	Weak transcription	Right Atrium	heart
2	chr10:112843800-112859400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:112845400-112861400	Weak transcription	Pancreas	Pancrea
4	chr10:112846000-112852200	Weak transcription	Ovary	ovary
5	chr10:112847200-112849800	Weak transcription	Stomach Mucosa	stomach
6	chr10:112849800-112850400	Enhancers	Duodenum Mucosa	Duodenum
7	chr10:112849800-112850400	Enhancers	Stomach Mucosa	stomach
8	chr10:112850400-112858600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr10:112852600-112854000	Enhancers	Stomach Mucosa	stomach
10	chr10:112852800-112854200	Enhancers	NHDF-Ad	bronchial
11	chr10:112853000-112854400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:112853200-112853800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:112853400-112854000	Enhancers	HSMM	muscle
14	chr10:112853600-112854000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:112854000-112858000	Weak transcription	Stomach Mucosa	stomach
16	chr10:112854200-112858200	Weak transcription	NHDF-Ad	bronchial
17	chr10:112854400-112858400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr10:112858000-112859800	Enhancers	Small Intestine	intestine
19	chr10:112858000-112865200	Enhancers	Stomach Mucosa	stomach
20	chr10:112858200-112858600	Enhancers	NHDF-Ad	bronchial
21	chr10:112858400-112859000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:112858600-112860000	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr10:112858600-112861200	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr10:112858600-112865200	Enhancers	Duodenum Mucosa	Duodenum
25	chr10:112859400-112859600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:112859400-112859600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr10:112859600-112860000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:112859600-112860800	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr10:112859800-112862200	Weak transcription	Small Intestine	intestine
30	chr10:112860000-112860200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr10:112860000-112860200	Enhancers	Fetal Intestine Large	intestine
32	chr10:112860000-112860600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
33	chr10:112860000-112860800	Enhancers	Fetal Muscle Trunk	muscle
34	chr10:112860000-112861000	Enhancers	Colonic Mucosa	Colon
35	chr10:112860200-112862400	Weak transcription	Fetal Intestine Large	intestine
36	chr10:112860200-112868200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr10:112860600-112861000	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr10:112860800-112862400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr10:112861000-112862000	Weak transcription	Colonic Mucosa	Colon
40	chr10:112861000-112862400	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr10:112861200-112862200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr10:112861400-112863800	Enhancers	Pancreas	Pancrea
43	chr10:112861600-112863600	Enhancers	Fetal Muscle Leg	muscle
44	chr10:112861800-112865200	Enhancers	Fetal Intestine Small	intestine
45	chr10:112862000-112862200	Enhancers	Liver	Liver
46	chr10:112862000-112863600	Enhancers	Colonic Mucosa	Colon
47	chr10:112862200-112863000	Enhancers	Small Intestine	intestine
48	chr10:112862200-112863400	Enhancers	Placenta	Placenta
49	chr10:112862200-112863600	Enhancers	Fetal Muscle Trunk	muscle
50	chr10:112862200-112864000	Enhancers	Rectal Mucosa Donor 31	rectum

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