Variant report

Variant	nsv881172
Chromosome Location	chr4:174772568-174873969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 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	chr4:174799973-174800234	K562	blood:	n/a	n/a
2	BCL3	chr4:174838292-174838609	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:174799922-174800199	K562	blood:	n/a	n/a
4	BHLHE40	chr4:174861367-174861570	K562	blood:	n/a	n/a
5	BHLHE40	chr4:174825762-174825772	K562	blood:	n/a	n/a
6	BRCA1	chr4:174851422-174851491	GM12878	blood:	n/a	n/a
7	CCNT2	chr4:174854015-174854176	K562	blood:	n/a	n/a
8	CEBPB	chr4:174783893-174784291	A549	lung:	n/a	chr4:174784114-174784125
9	CEBPB	chr4:174783884-174784274	HepG2	liver:	n/a	chr4:174784114-174784125
10	CEBPB	chr4:174830425-174830482	HepG2	liver:	n/a	chr4:174830471-174830482
11	CEBPB	chr4:174812256-174812582	IMR90	lung:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
12	CEBPB	chr4:174800035-174800200	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:174812280-174812558	K562	blood:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
14	CEBPB	chr4:174812282-174812586	HepG2	liver:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
15	CEBPB	chr4:174864742-174864995	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:174812281-174812585	A549	lung:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
17	CEBPB	chr4:174864666-174865010	K562	blood:	n/a	n/a
18	CEBPB	chr4:174783876-174784272	K562	blood:	n/a	chr4:174784114-174784125
19	CEBPB	chr4:174838322-174838686	IMR90	lung:	n/a	chr4:174838416-174838424
20	CEBPB	chr4:174799939-174800243	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:174814702-174814963	HepG2	liver:	n/a	chr4:174814834-174814845
22	CEBPB	chr4:174783928-174784265	Hela-S3	cervix:	n/a	chr4:174784114-174784125
23	CEBPB	chr4:174783874-174784258	IMR90	lung:	n/a	chr4:174784114-174784125
24	CEBPB	chr4:174857142-174857342	A549	lung:	n/a	n/a
25	CEBPB	chr4:174864681-174864902	K562	blood:	n/a	n/a
26	CEBPB	chr4:174857010-174857360	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:174864660-174865020	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr4:174784029-174784160	H1-hESC	embryonic stem cell:	n/a	chr4:174784114-174784125
29	CEBPD	chr4:174799832-174800224	K562	blood:	n/a	n/a
30	CREB1	chr4:174799920-174800122	A549	lung:	n/a	n/a
31	CTCF	chr4:174789770-174789840	ProgFib	skin:	n/a	n/a
32	CTCF	chr4:174785220-174785370	BE2_C	brain:	n/a	n/a
33	CTCF	chr4:174800660-174800810	BE2_C	brain:	n/a	n/a
34	CTCF	chr4:174797468-174797532	Fibrobl	skin:	n/a	n/a
35	CTCF	chr4:174864020-174864170	BE2_C	brain:	n/a	n/a
36	CTCF	chr4:174869873-174869963	ProgFib	skin:	n/a	n/a
37	CTCF	chr4:174842880-174843030	GM12866	blood:	n/a	n/a
38	CTCF	chr4:174864780-174865050	BE2_C	brain:	n/a	n/a
39	CTCF	chr4:174836200-174836350	GM12869	blood:	n/a	n/a
40	CTCF	chr4:174832254-174832363	ProgFib	skin:	n/a	n/a
41	CTCF	chr4:174785220-174785370	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:174785200-174785350	HMF	breast:	n/a	n/a
43	CTCF	chr4:174854095-174854136	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr4:174810117-174810164	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:174784400-174784550	HMF	breast:	n/a	n/a
46	CUX1	chr4:174801160-174801190	GM12878	blood:	n/a	n/a
47	E2F4	chr4:174819165-174819254	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr4:174773610-174773802	MCF10A-Er-Src	breast:	n/a	n/a
49	EGR1	chr4:174777139-174777366	K562	blood:	n/a	chr4:174777278-174777289 chr4:174777273-174777295 chr4:174777280-174777289 chr4:174777278-174777289 chr4:174777277-174777290 chr4:174777277-174777291 chr4:174777277-174777290 chr4:174777276-174777291 chr4:174777279-174777289 chr4:174777279-174777289 chr4:174777279-174777288 chr4:174777277-174777290
50	EGR1	chr4:174777145-174777331	K562	blood:	n/a	chr4:174777278-174777289 chr4:174777273-174777295 chr4:174777280-174777289 chr4:174777278-174777289 chr4:174777277-174777290 chr4:174777277-174777291 chr4:174777277-174777290 chr4:174777276-174777291 chr4:174777279-174777289 chr4:174777279-174777289 chr4:174777279-174777288 chr4:174777277-174777290

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:174859507..174861754-chr4:174865873..174868149,2	K562	blood:
2	chr4:174873733..174876256-chr4:174880533..174882266,2	K562	blood:
3	chr4:174867285..174870306-chr4:174877689..174880210,3	K562	blood:
4	chr4:174789438..174791902-chr4:174794071..174796664,2	K562	blood:
5	chr4:174864605..174866141-chr4:174866793..174868362,2	K562	blood:
6	chr4:174814123..174816648-chr4:174817513..174819556,2	K562	blood:
7	chr4:174859507..174861754-chr4:174865873..174868149,2	K562	blood:
8	chr4:174853099..174855885-chr4:174859341..174861783,2	K562	blood:
9	chr4:174850174..174852634-chr4:174855213..174858058,2	K562	blood:
10	chr4:174850174..174852634-chr4:174855213..174858058,2	K562	blood:
11	chr4:174665360..174668316-chr4:174784755..174786655,2	K562	blood:
12	chr4:174864605..174866141-chr4:174866793..174868362,2	K562	blood:
13	chr4:174853099..174855885-chr4:174859341..174861783,2	K562	blood:
14	chr4:174789438..174791902-chr4:174794071..174796664,2	K562	blood:
15	chr4:174633329..174636278-chr4:174857380..174860257,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO8-5	chr4:174845360-174846912	XLOC_004169
2	lnc-FBXO8-6	chr4:174821588-174821862	XLOC_004168
3	lnc-CEP44-4	chr4:174850376-174850610	NONHSAT099305
4	lnc-FBXO8-6	chr4:174834223-174834403	XLOC_004168
5	lnc-CEP44-4	chr4:174849646-174849795	NONHSAT099305
6	lnc-FBXO8-5	chr4:174849018-174849141	XLOC_004169
7	lnc-CEP44-7	chr4:174856883-174856923	l_2785_chr4:174856882-174860902_heart
8	lnc-CEP44-7	chr4:174859517-174860902	l_2785_chr4:174856882-174860902_heart
9	lnc-FBXO8-6	chr4:174798622-174798846	XLOC_004168
10	lnc-FBXO8-6	chr4:174824568-174824642	XLOC_004168
11	lnc-CEP44-4	chr4:174800521-174800556	l_2783_chr4:174800520-174818643_heart
12	lnc-CEP44-4	chr4:174849646-174849795	ENSG00000250708
13	lnc-CEP44-4	chr4:174850376-174850676	ENSG00000250708
14	lnc-FBXO8-6	chr4:174817545-174817876	XLOC_004168
15	lnc-FBXO8-6	chr4:174832952-174833046	XLOC_004168
16	lnc-FBXO8-8	chr4:174855643-174855858	l_2784_chr4:174852012-174855858_heart
17	lnc-FBXO8-5	chr4:174845358-174846912	ENSG00000251216
18	lnc-FBXO8-8	chr4:174852013-174855240	l_2784_chr4:174852012-174855858_heart
19	lnc-FBXO8-5	chr4:174849018-174849141	ENSG00000251216
20	lnc-CEP44-4	chr4:174818415-174818471	NONHSAT099305
21	lnc-CEP44-8	chr4:174849007-174849094	NONHSAT099307
22	lnc-CEP44-8	chr4:174852894-174852971	NONHSAT099307
23	lnc-FBXO8-6	chr4:174832952-174833093	XLOC_004168
24	lnc-CEP44-4	chr4:174818424-174818471	ENSG00000250708
25	lnc-CEP44-4	chr4:174816445-174818643	l_2783_chr4:174800520-174818643_heart
26	lnc-CEP44-4	chr4:174844263-174844432	NONHSAT099305
27	lnc-FBXO8-8	chr4:174856441-174856707	l_2784_chr4:174852012-174855858_heart
28	lnc-CEP44-8	chr4:174834518-174834597	NONHSAT099307

No data

Variant related genes	Relation type
ENSG00000250043	TF binding region
ENSG00000250708	TF binding region
ENSG00000250708	chromatin interactions

Extended variants
information (count: 2917 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2917 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144280756	chr4:174775606-174775607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573260985	chr4:174775608-174775609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs59180983	chr4:174775653-174775654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs561166653	chr4:174775770-174775771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369905014	chr4:174775779-174775780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189056483	chr4:174775780-174775781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181497204	chr4:174775781-174775782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117038306	chr4:174775804-174775805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552163861	chr4:174775813-174775814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142391101	chr4:174775838-174775839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185052270	chr4:174775895-174775896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115043144	chr4:174776019-174776020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568403803	chr4:174776023-174776024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537661301	chr4:174776070-174776071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80157021	chr4:174776123-174776124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72992147	chr4:174776128-174776129	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs537675102	chr4:174776129-174776130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189567387	chr4:174776154-174776155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539582908	chr4:174776168-174776169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180917619	chr4:174776194-174776195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150886399	chr4:174776201-174776202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535842325	chr4:174776231-174776232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72992148	chr4:174776244-174776245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185797012	chr4:174776264-174776265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116688890	chr4:174776292-174776293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191096329	chr4:174776346-174776347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113347026	chr4:174776377-174776378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6835851	chr4:174776461-174776462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs140098919	chr4:174776465-174776466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77864073	chr4:174776489-174776490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559018108	chr4:174776511-174776512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528114529	chr4:174776542-174776543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181835351	chr4:174776554-174776555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376059492	chr4:174776555-174776556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs56872852	chr4:174776630-174776631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531083607	chr4:174776665-174776666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186388828	chr4:174776670-174776671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190797613	chr4:174776689-174776690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556140443	chr4:174776699-174776700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145631114	chr4:174776703-174776704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147745884	chr4:174776708-174776709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183028774	chr4:174776733-174776734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566932082	chr4:174776766-174776767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs55747243	chr4:174776773-174776774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs142041374	chr4:174776820-174776821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13111698	chr4:174776834-174776835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141919442	chr4:174776868-174776869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372672522	chr4:174776894-174776895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557197103	chr4:174776937-174776938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535264847	chr4:174776977-174776978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Burkitt''s lymphoma	19759907	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174775600-174779000	Weak transcription	Aorta	Aorta
2	chr4:174779000-174779600	ZNF genes & repeats	Aorta	Aorta
3	chr4:174779000-174780800	Enhancers	Fetal Stomach	stomach
4	chr4:174780400-174781600	Enhancers	Fetal Heart	heart
5	chr4:174780600-174780800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:174793200-174794400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:174793400-174794200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:174795400-174811000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:174796800-174797200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr4:174796800-174797200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr4:174797000-174797200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr4:174797200-174800000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:174799200-174800600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:174799600-174800600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:174799800-174800600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:174799800-174802000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr4:174800000-174800600	Enhancers	Fetal Lung	lung
18	chr4:174800000-174800600	Enhancers	Placenta Amnion	Placenta Amnion
19	chr4:174800000-174801800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr4:174800200-174801600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:174800600-174801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:174800600-174801600	Weak transcription	Fetal Lung	lung
23	chr4:174800600-174804800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr4:174800600-174804800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:174801400-174802000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:174801600-174801800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:174801600-174813400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:174802000-174802200	Enhancers	Fetal Lung	lung
29	chr4:174802600-174803000	Weak transcription	Pancreas	Pancrea
30	chr4:174803000-174803200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:174803200-174803400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:174804800-174805000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:174804800-174805200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:174804800-174806000	Enhancers	Ovary	ovary
35	chr4:174804800-174806200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:174810800-174811400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:174811000-174811200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:174811400-174811600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:174813400-174813800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr4:174822800-174823000	Enhancers	Rectal Smooth Muscle	rectum
41	chr4:174823200-174824400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr4:174823800-174825400	Enhancers	Fetal Heart	heart
43	chr4:174824200-174824400	Enhancers	Stomach Smooth Muscle	stomach
44	chr4:174824400-174825600	Enhancers	Rectal Smooth Muscle	rectum
45	chr4:174825000-174825200	Enhancers	Stomach Smooth Muscle	stomach
46	chr4:174825400-174828200	Weak transcription	Fetal Heart	heart
47	chr4:174828200-174829000	Enhancers	Fetal Heart	heart
48	chr4:174828800-174829200	Enhancers	Gastric	stomach
49	chr4:174829000-174829200	Enhancers	Spleen	Spleen
50	chr4:174829000-174831200	Enhancers	Monocytes-CD14+_RO01746	blood

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