Variant report

Variant	nsv537295
Chromosome Location	chr4:149046598-149135489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:149113853-149113880	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:149094823-149095037	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr4:149098742-149098942	K562	blood:	n/a	n/a
4	CEBPB	chr4:149115806-149116117	HepG2	liver:	n/a	chr4:149115970-149115981
5	CEBPB	chr4:149061833-149062061	K562	blood:	n/a	n/a
6	CEBPB	chr4:149115821-149116134	IMR90	lung:	n/a	chr4:149115970-149115981
7	CHD2	chr4:149124593-149124988	H1-hESC	embryonic stem cell:	n/a	chr4:149124809-149124819
8	CTCF	chr4:149074120-149074270	BJ	skin:	n/a	n/a
9	CTCF	chr4:149074180-149074330	AG09319	gingival:	n/a	n/a
10	CTCF	chr4:149074200-149074350	HVMF	connective:	n/a	n/a
11	CTCF	chr4:149116454-149116642	K562	blood:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
12	CTCF	chr4:149074180-149074330	NHLF	lung:	n/a	n/a
13	CTCF	chr4:149047197-149047232	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr4:149116600-149116750	HVMF	connective:	n/a	n/a
15	CTCF	chr4:149116460-149116610	NHDF-neo	bronchial:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
16	CTCF	chr4:149074120-149074270	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr4:149092880-149093030	BE2_C	brain:	n/a	n/a
18	CTCF	chr4:149092840-149092990	NHEK	skin:	n/a	n/a
19	CTCF	chr4:149103620-149103770	AG04450	lung:	n/a	n/a
20	CTCF	chr4:149062910-149062930	GM10248	blood:	n/a	n/a
21	CTCF	chr4:149116420-149116570	HBMEC	blood vessel:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
22	CTCF	chr4:149074140-149074290	GM12878	blood:	n/a	n/a
23	CTCF	chr4:149056300-149056450	GM12872	blood:	n/a	n/a
24	CTCF	chr4:149092875-149092994	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr4:149061887-149061928	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr4:149074138-149074331	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:149056260-149056410	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr4:149116420-149116570	HPF	lung:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
29	CTCF	chr4:149061602-149061604	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:149116480-149116630	GM12867	blood:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
31	CTCF	chr4:149074120-149074270	AG04450	lung:	n/a	n/a
32	CTCF	chr4:149074220-149074370	RPTEC	kidney:	n/a	n/a
33	CTCF	chr4:149074100-149074250	HCM	heart:	n/a	n/a
34	CTCF	chr4:149116420-149116570	HFF	foreskin:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
35	CTCF	chr4:149073992-149074482	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:149116400-149116550	GM12864	blood:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
37	CTCF	chr4:149056280-149056430	BE2_C	brain:	n/a	n/a
38	CTCF	chr4:149056280-149056430	GM12870	blood:	n/a	n/a
39	CTCF	chr4:149071300-149071450	NHEK	skin:	n/a	n/a
40	CTCF	chr4:149071280-149071430	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr4:149071360-149071510	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:149092873-149092967	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:149074133-149074264	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr4:149074046-149074421	GM12878	blood:	n/a	n/a
45	CTCF	chr4:149074221-149074269	GM19239	blood:	n/a	n/a
46	CTCF	chr4:149116373-149116693	GM12878	blood:	n/a	chr4:149116529-149116547 chr4:149116530-149116546 chr4:149116524-149116545
47	CTCF	chr4:149074200-149074265	ProgFib	skin:	n/a	n/a
48	CTCF	chr4:149066808-149066857	MCF-7	breast:	n/a	chr4:149066811-149066829 chr4:149066813-149066826 chr4:149066818-149066826 chr4:149066820-149066833
49	CTCF	chr4:149074160-149074310	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr4:149074100-149074250	BE2_C	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:149074093-149074143	HMEC	breast:	n/a
2	chr4:149074093-149074143	ECC-1	luminal epithelium:	n/a
3	chr4:149074093-149074143	HEK293	kidney:	embryo
4	chr4:149074093-149074143	PANC-1	pancreas:	n/a
5	chr4:149074093-149074143	GM12892	blood:	n/a
6	chr4:149083955-149084005	PANC-1	pancreas:	n/a
7	chr4:149074093-149074143	AG04450	lung:	fetal
8	chr4:149083955-149084005	SKMC	muscle:	n/a
9	chr4:149074093-149074143	AG09319	gingival:	n/a
10	chr4:149074093-149074143	NT2-D1	testis:	n/a
11	chr4:149083955-149084005	ECC-1	luminal epithelium:	n/a
12	chr4:149083955-149084005	GM12891	blood:	n/a
13	chr4:149083955-149084005	GM12878	blood:	n/a
14	chr4:149083955-149084005	Hepatocyte	liver:	n/a
15	chr4:149083955-149084005	HCM	heart:	n/a
16	chr4:149083955-149084005	HL-60	blood:	n/a
17	chr4:149083955-149084005	U87	brain:	n/a
18	chr4:149074093-149074143	AG09309	skin:	n/a
19	chr4:149083955-149084005	HCF	heart:	n/a
20	chr4:149083955-149084005	GM12892	blood:	n/a
21	chr4:149074093-149074143	SAEC	small airway:	n/a
22	chr4:149083955-149084005	NHBE	bronchial:	n/a
23	chr4:149074093-149074143	GM12891	blood:	n/a
24	chr4:149074093-149074143	HNPCEpiC	eye:	n/a
25	chr4:149074093-149074143	GM19239	blood:	n/a
26	chr4:149083955-149084005	BE2_C	brain:	n/a
27	chr4:149083955-149084005	PFSK-1	brain:	n/a
28	chr4:149074093-149074143	AoSMC	blood vessel:	n/a
29	chr4:149083955-149084005	HRE	kidney:	n/a
30	chr4:149074093-149074143	BJ	skin:	n/a
31	chr4:149074093-149074143	Hela-S3	cervix:	n/a
32	chr4:149074093-149074143	BE2_C	brain:	n/a
33	chr4:149083955-149084005	H1-hESC	embryonic stem cell:	embryo
34	chr4:149083955-149084005	SAEC	small airway:	n/a
35	chr4:149083955-149084005	HEEpiC	esophagus:	n/a
36	chr4:149074093-149074143	HRE	kidney:	n/a
37	chr4:149074093-149074143	Caco-2	colon:	n/a
38	chr4:149083955-149084005	HIPEpiC	eye:	n/a
39	chr4:149074093-149074143	LNCaP	prostate:	n/a
40	chr4:149074093-149074143	A549	lung:	n/a
41	chr4:149074093-149074143	U87	brain:	n/a
42	chr4:149083955-149084005	HMEC	breast:	n/a
43	chr4:149074093-149074143	HEEpiC	esophagus:	n/a
44	chr4:149083955-149084005	AG04450	lung:	fetal
45	chr4:149074093-149074143	MCF-7	breast:	n/a
46	chr4:149074093-149074143	NB4	blood:	n/a
47	chr4:149083955-149084005	LNCaP	prostate:	n/a
48	chr4:149083955-149084005	CMK	blood:	n/a
49	chr4:149083955-149084005	NT2-D1	testis:	n/a
50	chr4:149074093-149074143	HL-60	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:149120620..149122902-chr4:149123252..149125690,3	K562	blood:
2	chr4:149120620..149122902-chr4:149123483..149125690,2	K562	blood:
3	chr4:148844312..148847259-chr4:149048458..149051451,2	MCF-7	breast:
4	chr4:148904893..148905747-chr4:149073698..149074268,3	MCF-7	breast:
5	chr4:148846022..148846608-chr4:149073964..149074698,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP10-1	chr4:149129143-149129413	ENSG00000250354.1
2	lnc-ARHGAP10-1	chr4:149067622-149067700	ENSG00000250354.1
3	lnc-ARHGAP10-1	chr4:149129702-149130031	ENSG00000250354.1

No data

Variant related genes	Relation type
ENSG00000250354	TF binding region
NR3C2	TF binding region
ENSG00000250354	CpG island
NR3C2	CpG island
ENSG00000151623	chromatin interactions

Extended variants
information (count: 3329 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3329 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531386035	chr4:149046605-149046606	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551299587	chr4:149046643-149046644	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74523730	chr4:149046653-149046654	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539821478	chr4:149046660-149046661	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115055343	chr4:149046672-149046673	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183247223	chr4:149046689-149046690	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535605132	chr4:149046690-149046691	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375169373	chr4:149046727-149046728	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143926064	chr4:149046747-149046748	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368452228	chr4:149046750-149046751	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544816122	chr4:149046761-149046762	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558303873	chr4:149046768-149046769	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374631438	chr4:149046788-149046789	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578240003	chr4:149046812-149046813	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4447838	chr4:149046846-149046847	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186964966	chr4:149046851-149046852	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367627762	chr4:149046855-149046856	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559864789	chr4:149046886-149046887	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113984211	chr4:149046911-149046912	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184001986	chr4:149046942-149046943	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570329771	chr4:149046947-149046948	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552965874	chr4:149046988-149046989	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371419887	chr4:149047090-149047091	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537682603	chr4:149047096-149047097	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368093246	chr4:149047120-149047121	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186907011	chr4:149047141-149047142	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551112692	chr4:149047142-149047143	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571216458	chr4:149047178-149047179	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527555871	chr4:149047179-149047180	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75297062	chr4:149047194-149047195	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148617333	chr4:149047195-149047196	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142075648	chr4:149047196-149047197	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555944773	chr4:149047269-149047270	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555961906	chr4:149047381-149047382	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191319089	chr4:149047401-149047402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182732564	chr4:149047405-149047406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558351559	chr4:149047407-149047408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187015885	chr4:149047425-149047426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577021238	chr4:149047444-149047445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150264104	chr4:149047460-149047461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146177779	chr4:149047472-149047473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193157267	chr4:149047515-149047516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573593687	chr4:149047516-149047517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541448546	chr4:149047525-149047526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6815979	chr4:149047581-149047582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185350762	chr4:149047607-149047608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111937522	chr4:149047661-149047662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562246908	chr4:149047722-149047723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112786787	chr4:149047756-149047757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544818751	chr4:149047762-149047763	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
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149004600-149052400	Weak transcription	Esophagus	oesophagus
2	chr4:149018000-149085800	Weak transcription	Stomach Mucosa	stomach
3	chr4:149024000-149068600	Weak transcription	Right Ventricle	heart
4	chr4:149030800-149067000	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr4:149033800-149047000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr4:149035400-149048200	Weak transcription	Brain Angular Gyrus	brain
7	chr4:149039400-149069400	Weak transcription	Colonic Mucosa	Colon
8	chr4:149040600-149083200	Weak transcription	Gastric	stomach
9	chr4:149041400-149067600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:149041400-149092000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr4:149041600-149047200	Weak transcription	Pancreas	Pancrea
12	chr4:149041600-149061400	Weak transcription	Fetal Stomach	stomach
13	chr4:149041600-149069600	Weak transcription	Brain Anterior Caudate	brain
14	chr4:149041800-149074400	Weak transcription	Lung	lung
15	chr4:149044600-149046600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
16	chr4:149044800-149047400	ZNF genes & repeats	Liver	Liver
17	chr4:149045400-149047400	ZNF genes & repeats	Fetal Muscle Leg	muscle
18	chr4:149045600-149104800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr4:149046200-149046600	ZNF genes & repeats	Brain Substantia Nigra	brain
20	chr4:149046200-149046600	ZNF genes & repeats	Ovary	ovary
21	chr4:149046400-149046600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr4:149046400-149046600	ZNF genes & repeats	Aorta	Aorta
23	chr4:149046400-149046600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
24	chr4:149046400-149047200	Weak transcription	Psoas Muscle	Psoas
25	chr4:149046400-149047400	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr4:149046400-149076600	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr4:149046400-149085800	Weak transcription	Rectal Smooth Muscle	rectum
28	chr4:149046600-149048200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr4:149046600-149055400	Weak transcription	Brain Substantia Nigra	brain
30	chr4:149046600-149066600	Weak transcription	Ovary	ovary
31	chr4:149046600-149075600	Weak transcription	Duodenum Mucosa	Duodenum
32	chr4:149046600-149087400	Weak transcription	Aorta	Aorta
33	chr4:149047000-149047200	Enhancers	Primary T cells from cord blood	blood
34	chr4:149047000-149051800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr4:149047000-149066800	Weak transcription	Fetal Muscle Trunk	muscle
36	chr4:149047000-149077200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr4:149047200-149047400	ZNF genes & repeats	Left Ventricle	heart
38	chr4:149047200-149047400	ZNF genes & repeats	Pancreas	Pancrea
39	chr4:149047200-149047400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
40	chr4:149047200-149047400	ZNF genes & repeats	Small Intestine	intestine
41	chr4:149047400-149049200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:149047400-149049400	Weak transcription	Liver	Liver
43	chr4:149047400-149049800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr4:149047400-149062600	Weak transcription	Fetal Muscle Leg	muscle
45	chr4:149047400-149066000	Weak transcription	Pancreas	Pancrea
46	chr4:149047400-149067200	Weak transcription	Left Ventricle	heart
47	chr4:149047400-149083800	Weak transcription	Small Intestine	intestine
48	chr4:149047600-149052200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr4:149047800-149048000	Enhancers	Primary T cells from cord blood	blood
50	chr4:149048200-149048800	Enhancers	Duodenum Smooth Muscle	Duodenum

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