Variant report

Variant	nsv470083
Chromosome Location	chr4:149817052-149903982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:149896761-149897011	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:149819586-149819774	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr4:149828000-149828150	NHEK	skin:	n/a	chr4:149828107-149828125 chr4:149828113-149828122
4	CTCF	chr4:149902144-149902214	LNCaP	prostate:	n/a	n/a
5	CTCF	chr4:149850137-149850194	Lung_OC	lung:	n/a	n/a
6	CTCF	chr4:149822300-149822450	BE2_C	brain:	n/a	n/a
7	CTCF	chr4:149818903-149818954	Spleen_OC	spleen:	n/a	n/a
8	CTCF	chr4:149818323-149818353	GM13976	blood:	n/a	n/a
9	CTCF	chr4:149820324-149820378	GM10248	blood:	n/a	n/a
10	CTCF	chr4:149822415-149822450	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr4:149822342-149822524	GM12878	blood:	n/a	n/a
12	CTCF	chr4:149821080-149821230	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr4:149822340-149822490	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr4:149851934-149851993	GM10248	blood:	n/a	n/a
15	CTCF	chr4:149829255-149829310	LNCaP	prostate:	n/a	n/a
16	CTCF	chr4:149822360-149822510	RPTEC	kidney:	n/a	n/a
17	CTCF	chr4:149891735-149891765	Fibrobl	skin:	n/a	n/a
18	CTCF	chr4:149822340-149822490	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr4:149864568-149864592	Lung_OC	lung:	n/a	n/a
20	E2F4	chr4:149840954-149841157	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr4:149877511-149877671	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr4:149827364-149827418	MCF10A-Er-Src	breast:	n/a	n/a
23	ELK1	chr4:149885870-149885993	GM12878	blood:	n/a	n/a
24	ESR1	chr4:149875093-149875421	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr4:149876716-149877106	ECC-1	luminal epithelium:	n/a	n/a
26	FAM48A	chr4:149827190-149827325	GM12878	blood:	n/a	n/a
27	FOS	chr4:149847980-149848300	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr4:149877163-149877414	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:149884148-149884481	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:149872551-149872918	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr4:149877118-149877338	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:149848075-149848361	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr4:149838420-149838863	MCF10A-Er-Src	breast:	n/a	chr4:149838746-149838756 chr4:149838730-149838739 chr4:149838746-149838756 chr4:149838638-149838645 chr4:149838746-149838756 chr4:149838636-149838645
34	FOS	chr4:149877188-149877388	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:149872549-149872916	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:149872565-149872898	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr4:149848057-149848293	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr4:149848079-149848347	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:149838587-149838854	MCF10A-Er-Src	breast:	n/a	chr4:149838746-149838756 chr4:149838730-149838739 chr4:149838746-149838756 chr4:149838638-149838645 chr4:149838746-149838756 chr4:149838636-149838645
40	FOS	chr4:149875385-149875547	MCF10A-Er-Src	breast:	n/a	chr4:149875460-149875468
41	FOS	chr4:149838615-149838794	MCF10A-Er-Src	breast:	n/a	chr4:149838746-149838756 chr4:149838730-149838739 chr4:149838746-149838756 chr4:149838638-149838645 chr4:149838746-149838756 chr4:149838636-149838645
42	FOS	chr4:149872553-149872903	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr4:149877106-149877417	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:149884141-149884441	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:149884167-149884423	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:149884155-149884434	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:149831528-149831537	MCF10A-Er-Src	breast:	n/a	n/a
48	FOSL1	chr4:149877037-149877428	HCT-116	colon:	n/a	n/a
49	FOXA1	chr4:149859490-149859816	T-47D	breast:	n/a	n/a
50	GATA3	chr4:149859461-149859903	MCF-7	breast:	n/a	chr4:149859710-149859731

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:149822936-149822986	ovcar-3	ovarian:	n/a
2	chr4:149822936-149822986	GM12892	blood:	n/a
3	chr4:149822936-149822986	GM12878	blood:	n/a
4	chr4:149822936-149822986	HepG2	liver:	n/a
5	chr4:149822936-149822986	NHDF-neo	bronchial:	n/a
6	chr4:149822936-149822986	Hela-S3	cervix:	n/a
7	chr4:149822936-149822986	GM12891	blood:	n/a
8	chr4:149822936-149822986	PrEC	prostate:	n/a
9	chr4:149822936-149822986	MCF10A-Er-Src	breast:	n/a
10	chr4:149822936-149822986	MCF-7	breast:	n/a
11	chr4:149822936-149822986	HEK293	kidney:	embryo
12	chr4:149822936-149822986	PFSK-1	brain:	n/a
13	chr4:149822936-149822986	LNCaP	prostate:	n/a
14	chr4:149822936-149822986	HCM	heart:	n/a
15	chr4:149822936-149822986	BJ	skin:	n/a
16	chr4:149822936-149822986	HRCEpiC	kidney:	n/a
17	chr4:149822936-149822986	NT2-D1	testis:	n/a
18	chr4:149822936-149822986	HEEpiC	esophagus:	n/a
19	chr4:149822936-149822986	AG09319	gingival:	n/a
20	chr4:149822936-149822986	NH-A	brain:	n/a
21	chr4:149822936-149822986	HCF	heart:	n/a
22	chr4:149822936-149822986	ProgFib	skin:	n/a
23	chr4:149822936-149822986	ECC-1	luminal epithelium:	n/a
24	chr4:149822936-149822986	A549	lung:	n/a
25	chr4:149822936-149822986	NB4	blood:	n/a
26	chr4:149822936-149822986	HRPEpiC	eye:	n/a
27	chr4:149822936-149822986	HL-60	blood:	n/a
28	chr4:149822936-149822986	AG04450	lung:	fetal
29	chr4:149822936-149822986	SAEC	small airway:	n/a
30	chr4:149822936-149822986	HNPCEpiC	eye:	n/a
31	chr4:149822936-149822986	GM19239	blood:	n/a
32	chr4:149822936-149822986	NHBE	bronchial:	n/a
33	chr4:149822936-149822986	PANC-1	pancreas:	n/a
34	chr4:149822936-149822986	RPTEC	kidney:	n/a
35	chr4:149822936-149822986	HAEpiC	amniotic membrane:	n/a
36	chr4:149822936-149822986	Jurkat	blood:	n/a
37	chr4:149822936-149822986	CMK	blood:	n/a
38	chr4:149822936-149822986	AG10803	skin:	n/a
39	chr4:149822936-149822986	Hepatocyte	liver:	n/a
40	chr4:149822936-149822986	HCT-116	colon:	n/a
41	chr4:149822936-149822986	SK-N-SH	brain:	n/a
42	chr4:149822936-149822986	U87	brain:	n/a
43	chr4:149822936-149822986	Caco-2	colon:	n/a
44	chr4:149822936-149822986	HRE	kidney:	n/a
45	chr4:149822936-149822986	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:149822936-149822986	K562	blood:	n/a
47	chr4:149822936-149822986	SKMC	muscle:	n/a
48	chr4:149822936-149822986	HCPEpiC	choroid plexus:	n/a
49	chr4:149822936-149822986	HIPEpiC	eye:	n/a
50	chr4:149822936-149822986	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:149855945..149858873-chr4:149859035..149861615,2	K562	blood:
2	chr4:149855945..149858873-chr4:149859035..149861615,2	K562	blood:
3	chr17:56988283..56990164-chr4:149864191..149866506,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP10-4	chr4:149840726-149840925	l_2751_chr4:149833600-149840763_testes
2	lnc-NR3C2-2	chr4:149862809-149862994	XLOC_004118
3	lnc-NR3C2-2	chr4:149863494-149863530	XLOC_004118
4	lnc-NR3C2-2	chr4:149862700-149862929	ENSG00000249317
5	lnc-NR3C2-2	chr4:149862101-149862239	ENSG00000249317
6	lnc-NR3C2-2	chr4:149862093-149862239	XLOC_004118
7	lnc-ARHGAP10-4	chr4:149833601-149833859	l_2751_chr4:149833600-149840763_testes

No data

Variant related genes	Relation type
ENSG00000249317	TF binding region
ENSG00000249317	CpG island
SETD7	miRNA target sites
GNG12	miRNA target sites

Extended variants
information (count: 1901 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1901 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2520496	chr4:149817052-149817053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544416555	chr4:149817069-149817070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563657227	chr4:149817112-149817113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183852228	chr4:149817150-149817151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188415402	chr4:149817151-149817152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142809298	chr4:149817273-149817274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528760313	chr4:149817333-149817334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548435923	chr4:149817343-149817344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568407770	chr4:149817353-149817354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554349026	chr4:149817370-149817371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531059595	chr4:149817381-149817382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191335336	chr4:149817388-149817389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570489885	chr4:149817404-149817405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76671070	chr4:149817430-149817431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373490966	chr4:149817433-149817434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112405072	chr4:149817475-149817476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60476529	chr4:149817489-149817490	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535433940	chr4:149817490-149817491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555744781	chr4:149817516-149817517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575587692	chr4:149817519-149817520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78154766	chr4:149817553-149817554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538071659	chr4:149817564-149817565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17025399	chr4:149817565-149817566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577286480	chr4:149817592-149817593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546230192	chr4:149817601-149817602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559494824	chr4:149817626-149817627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113952640	chr4:149817670-149817671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539654976	chr4:149817671-149817672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116081343	chr4:149817682-149817683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184331322	chr4:149817714-149817715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs853695	chr4:149817820-149817821	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558488794	chr4:149817832-149817833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564675216	chr4:149817853-149817854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56338121	chr4:149817891-149817892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369487629	chr4:149817920-149817921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532889957	chr4:149817971-149817972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188631877	chr4:149818018-149818019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs862655	chr4:149818019-149818020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs140660639	chr4:149818072-149818073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs578136619	chr4:149818085-149818086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369362846	chr4:149818097-149818098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181745454	chr4:149818232-149818233	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569188515	chr4:149818246-149818247	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533914072	chr4:149818252-149818253	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538108423	chr4:149818270-149818271	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75672793	chr4:149818294-149818295	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372363075	chr4:149818331-149818332	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574072484	chr4:149818346-149818347	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185085775	chr4:149818358-149818359	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572981268	chr4:149818362-149818363	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149814800-149819600	Weak transcription	Stomach Mucosa	stomach
2	chr4:149818200-149819600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:149818800-149819600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr4:149819200-149819600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
5	chr4:149819200-149819600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:149819600-149822200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr4:149819600-149822200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:149821800-149823200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr4:149821800-149823200	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr4:149822000-149822200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:149822000-149822800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:149822000-149823200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr4:149822000-149823200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr4:149822000-149823400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:149822000-149823400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:149822200-149822400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:149822200-149823000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:149822200-149823200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:149822600-149823000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:149822800-149823000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:149823000-149823200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr4:149823000-149824000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:149824600-149824800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:149825200-149826600	Enhancers	Stomach Mucosa	stomach
25	chr4:149826000-149826800	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:149827000-149827400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr4:149828200-149828600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:149831000-149831600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:149834000-149844800	Weak transcription	Stomach Mucosa	stomach
30	chr4:149843200-149844400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr4:149844400-149845400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr4:149844600-149845200	Enhancers	Duodenum Smooth Muscle	Duodenum
33	chr4:149844800-149845600	Enhancers	Stomach Mucosa	stomach
34	chr4:149845000-149845400	Enhancers	Fetal Stomach	stomach
35	chr4:149845400-149845800	Weak transcription	Fetal Stomach	stomach
36	chr4:149845400-149845800	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr4:149845600-149846200	Enhancers	Stomach Smooth Muscle	stomach
38	chr4:149845600-149847800	Weak transcription	Stomach Mucosa	stomach
39	chr4:149845800-149846000	Enhancers	Fetal Stomach	stomach
40	chr4:149846000-149847600	Weak transcription	Fetal Stomach	stomach
41	chr4:149846200-149846600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr4:149846400-149848600	Enhancers	Fetal Muscle Leg	muscle
43	chr4:149846600-149847200	Enhancers	Stomach Smooth Muscle	stomach
44	chr4:149847000-149848800	Enhancers	Fetal Brain Male	brain
45	chr4:149847200-149847400	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr4:149847200-149848600	Enhancers	Brain Germinal Matrix	brain
47	chr4:149847400-149848200	Enhancers	Stomach Smooth Muscle	stomach
48	chr4:149847600-149848000	Enhancers	HSMMtube	muscle
49	chr4:149847600-149848400	Enhancers	Fetal Stomach	stomach
50	chr4:149847800-149848000	Enhancers	Rectal Mucosa Donor 31	rectum

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