Variant report

Variant	nsv1031914
Chromosome Location	chr5:118516878-118589497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:155)
CpG islands
(count:123)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:155 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118565756-118565843	K562	blood:	n/a	n/a
2	ARID3A	chr5:118554812-118555173	HepG2	liver:	n/a	n/a
3	ATF2	chr5:118556197-118556741	GM12878	blood:	n/a	n/a
4	ATF2	chr5:118556225-118556630	GM12878	blood:	n/a	n/a
5	ATF3	chr5:118523560-118523863	GM12878	blood:	n/a	chr5:118523740-118523749
6	CEBPB	chr5:118526538-118526738	K562	blood:	n/a	n/a
7	CEBPB	chr5:118586900-118587201	IMR90	lung:	n/a	chr5:118587063-118587074
8	CEBPB	chr5:118533208-118533331	HepG2	liver:	n/a	chr5:118533223-118533234
9	CEBPB	chr5:118551438-118551493	IMR90	lung:	n/a	chr5:118551454-118551465
10	CEBPB	chr5:118586985-118587207	HepG2	liver:	n/a	chr5:118587063-118587074
11	CEBPB	chr5:118586982-118587245	A549	lung:	n/a	chr5:118587063-118587074
12	CEBPB	chr5:118579154-118579159	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:118551405-118551516	HepG2	liver:	n/a	chr5:118551454-118551465
14	CTCF	chr5:118545128-118545135	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:118547892-118547952	HepG2	liver:	n/a	n/a
16	CTCF	chr5:118566300-118566450	A549	lung:	n/a	n/a
17	CTCF	chr5:118547900-118548050	A549	lung:	n/a	n/a
18	CTCF	chr5:118547839-118548001	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr5:118519759-118519762	GM10248	blood:	n/a	n/a
20	CTCF	chr5:118587980-118588130	NHLF	lung:	n/a	n/a
21	CTCF	chr5:118547760-118547910	HCT-116	colon:	n/a	n/a
22	CTCF	chr5:118547901-118547907	GM19240	blood:	n/a	n/a
23	CTCF	chr5:118586839-118586859	GM10266	blood:	n/a	n/a
24	CTCF	chr5:118547871-118547972	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr5:118547657-118548180	HCT-116	colon:	n/a	n/a
26	CTCF	chr5:118547861-118547951	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:118547700-118547850	HCT-116	colon:	n/a	n/a
28	CTCF	chr5:118547845-118547945	HepG2	liver:	n/a	n/a
29	CUX1	chr5:118556435-118556468	GM12878	blood:	n/a	n/a
30	E2F4	chr5:118532083-118532158	MCF10A-Er-Src	breast:	n/a	n/a
31	EP300	chr5:118556360-118556607	GM12878	blood:	n/a	chr5:118556441-118556455
32	EP300	chr5:118536653-118536698	K562	blood:	n/a	n/a
33	EP300	chr5:118526386-118526671	K562	blood:	n/a	n/a
34	EP300	chr5:118556395-118556607	GM12878	blood:	n/a	chr5:118556441-118556455
35	FAM48A	chr5:118528316-118528390	GM12878	blood:	n/a	n/a
36	FOS	chr5:118586987-118587552	MCF10A-Er-Src	breast:	n/a	chr5:118587385-118587397
37	FOS	chr5:118579824-118579987	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr5:118579728-118579902	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr5:118587030-118587304	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr5:118587008-118587208	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr5:118554974-118555108	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr5:118554954-118555128	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr5:118586960-118587294	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr5:118554976-118555172	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr5:118579827-118579864	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL2	chr5:118565590-118566075	A549	lung:	n/a	n/a
47	FOXA1	chr5:118580059-118580329	T-47D	breast:	n/a	n/a
48	FOXA1	chr5:118580022-118580381	T-47D	breast:	n/a	n/a
49	FOXA1	chr5:118554763-118555143	HepG2	liver:	n/a	n/a
50	FOXA2	chr5:118565615-118566003	A549	lung:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118584299-118584349	NH-A	brain:	n/a
2	chr5:118584299-118584349	NH-A	brain:	n/a
3	chr5:118584299-118584349	HUVEC	blood vessel:	n/a
4	chr5:118584299-118584349	MCF10A-Er-Src	breast:	n/a
5	chr5:118580164-118580214	A549	lung:	n/a
6	chr5:118580164-118580214	HL-60	blood:	n/a
7	chr5:118584299-118584349	AG09319	gingival:	n/a
8	chr5:118580164-118580214	AG04450	lung:	fetal
9	chr5:118584299-118584349	HCM	heart:	n/a
10	chr5:118580164-118580214	SK-N-MC	brain:	n/a
11	chr5:118580164-118580214	PFSK-1	brain:	n/a
12	chr5:118580164-118580214	HRCEpiC	kidney:	n/a
13	chr5:118580164-118580214	HCPEpiC	choroid plexus:	n/a
14	chr5:118580164-118580214	AG04449	skin:	fetal
15	chr5:118584299-118584349	Caco-2	colon:	n/a
16	chr5:118580164-118580214	CMK	blood:	n/a
17	chr5:118580164-118580214	HRPEpiC	eye:	n/a
18	chr5:118584299-118584349	HRCEpiC	kidney:	n/a
19	chr5:118584299-118584349	AoSMC	blood vessel:	n/a
20	chr5:118580164-118580214	BE2_C	brain:	n/a
21	chr5:118580164-118580214	ProgFib	skin:	n/a
22	chr5:118580164-118580214	U87	brain:	n/a
23	chr5:118584299-118584349	BE2_C	brain:	n/a
24	chr5:118580164-118580214	HIPEpiC	eye:	n/a
25	chr5:118580164-118580214	SK-N-SH	brain:	n/a
26	chr5:118584299-118584349	SK-N-SH	brain:	n/a
27	chr5:118580164-118580214	NHDF-neo	bronchial:	n/a
28	chr5:118580164-118580214	LNCaP	prostate:	n/a
29	chr5:118584299-118584349	HRPEpiC	eye:	n/a
30	chr5:118580164-118580214	Caco-2	colon:	n/a
31	chr5:118584299-118584349	MCF-7	breast:	n/a
32	chr5:118580164-118580214	Hepatocyte	liver:	n/a
33	chr5:118580164-118580214	HEK293	kidney:	embryo
34	chr5:118584299-118584349	AG04449	skin:	fetal
35	chr5:118584299-118584349	HEEpiC	esophagus:	n/a
36	chr5:118580164-118580214	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:118584299-118584349	NHBE	bronchial:	n/a
38	chr5:118584299-118584349	RPTEC	kidney:	n/a
39	chr5:118580164-118580214	HepG2	liver:	n/a
40	chr5:118584299-118584349	HCF	heart:	n/a
41	chr5:118580164-118580214	K562	blood:	n/a
42	chr5:118584299-118584349	SAEC	small airway:	n/a
43	chr5:118580164-118580214	HEEpiC	esophagus:	n/a
44	chr5:118584299-118584349	AG09309	skin:	n/a
45	chr5:118584299-118584349	SKMC	muscle:	n/a
46	chr5:118580164-118580214	GM19239	blood:	n/a
47	chr5:118584299-118584349	SK-N-MC	brain:	n/a
48	chr5:118580164-118580214	HCT-116	colon:	n/a
49	chr5:118580164-118580214	SAEC	small airway:	n/a
50	chr5:118584299-118584349	HNPCEpiC	eye:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118564790..118566564-chr5:118567290..118569739,2	MCF-7	breast:
2	chr5:118565495..118568249-chr5:118569908..118571816,2	K562	blood:
3	chr5:118574799..118576857-chr5:118580303..118583195,3	K562	blood:
4	chr5:118581886..118584543-chr5:118587332..118589504,3	K562	blood:
5	chr5:118560242..118562661-chr5:118578972..118580567,2	MCF-7	breast:
6	chr5:118547822..118550227-chr5:118558352..118560676,2	K562	blood:
7	chr5:118583005..118584543-chr5:118587332..118589504,2	K562	blood:
8	chr5:118581886..118584543-chr5:118587332..118589504,3	K562	blood:
9	chr5:118574634..118576211-chr5:118609734..118611582,2	MCF-7	breast:
10	chr5:118551365..118552971-chr5:118559798..118561455,2	K562	blood:
11	chr5:118580319..118581889-chr5:118587199..118590009,2	K562	blood:
12	chr5:118549930..118551447-chr5:118556250..118558321,2	K562	blood:
13	chr5:118547322..118548106-chr5:118670433..118671294,2	MCF-7	breast:
14	chr5:118559931..118561681-chr5:118573436..118576186,2	K562	blood:
15	chr5:118548598..118551453-chr5:118553322..118554885,2	MCF-7	breast:
16	chr5:118567020..118569794-chr5:118587970..118590169,2	K562	blood:
17	chr5:118582682..118585597-chr5:118588093..118590395,3	MCF-7	breast:
18	chr5:118547822..118550227-chr5:118558352..118560676,2	K562	blood:
19	chr5:118567020..118569794-chr5:118587970..118590169,2	K562	blood:
20	chr5:118580319..118581889-chr5:118587199..118590009,2	K562	blood:
21	chr5:118559801..118561992-chr5:118562252..118565088,2	K562	blood:
22	chr5:118586532..118588054-chr5:118602135..118604215,2	K562	blood:
23	chr5:118583005..118584543-chr5:118587332..118589504,2	K562	blood:
24	chr5:118581217..118584329-chr5:118602907..118604848,3	K562	blood:
25	chr5:118573504..118576319-chr5:118580787..118583650,2	K562	blood:
26	chr5:118542220..118543849-chr5:118544632..118547228,2	K562	blood:
27	chr5:118549930..118551447-chr5:118556250..118558321,2	K562	blood:
28	chr5:118570748..118572621-chr5:118572841..118575732,2	MCF-7	breast:
29	chr5:118559931..118561681-chr5:118573436..118576186,2	K562	blood:
30	chr5:118553070..118555553-chr5:118571329..118573313,2	K562	blood:
31	chr5:118549863..118550376-chr7:16168238..16169156,2	MCF-7	breast:
32	chr5:118542220..118543849-chr5:118544632..118547228,2	K562	blood:
33	chr5:118551365..118552971-chr5:118559798..118561455,2	K562	blood:
34	chr5:118574799..118576857-chr5:118580303..118583195,3	K562	blood:
35	chr5:118571373..118573245-chr5:118582858..118585572,2	K562	blood:
36	chr5:118573504..118576319-chr5:118580787..118583650,2	K562	blood:
37	chr5:118560242..118562661-chr5:118578972..118580567,2	MCF-7	breast:
38	chr5:118565495..118568249-chr5:118569908..118571816,2	K562	blood:
39	chr5:118582682..118585597-chr5:118588093..118590395,3	MCF-7	breast:
40	chr5:118559801..118561992-chr5:118562252..118565088,2	K562	blood:
41	chr5:118564790..118566564-chr5:118567290..118569739,2	MCF-7	breast:
42	chr5:118548598..118551453-chr5:118553322..118554885,2	MCF-7	breast:
43	chr5:118579079..118581230-chr5:118604088..118605942,2	MCF-7	breast:
44	chr5:118503506..118505330-chr5:118525953..118528174,2	K562	blood:
45	chr5:118583032..118585646-chr5:118590465..118591965,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	DMXL1	hsa-miR-92a-3p	chr5:118584515-118584522
2	DMXL1	hsa-miR-92a-3p	chr5:118584501-118584522
3	DMXL1	hsa-miR-9-5p	chr5:118584038-118584059

Variant related genes	Relation type
DMXL1	TF binding region
DMXL1	CpG island
ENSG00000172869	chromatin interactions
ENSG00000145779	chromatin interactions

Extended variants
information (count: 2835 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2835 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3923326	chr5:118516878-118516879	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34074459	chr5:118516886-118516887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562101942	chr5:118516887-118516888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575314789	chr5:118516899-118516900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577267980	chr5:118516908-118516909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7727906	chr5:118516913-118516914	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs534388124	chr5:118516916-118516917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78601311	chr5:118516949-118516950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138416882	chr5:118516956-118516957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77671608	chr5:118516989-118516990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149276653	chr5:118516994-118516995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146111301	chr5:118517066-118517067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115700559	chr5:118517092-118517093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139370942	chr5:118517126-118517127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192974542	chr5:118517128-118517129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142171238	chr5:118517166-118517167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550644645	chr5:118517172-118517173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374324532	chr5:118517199-118517200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570551371	chr5:118517249-118517250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539444279	chr5:118517256-118517257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552902549	chr5:118517296-118517297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146392234	chr5:118517380-118517381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535741831	chr5:118517388-118517389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549565731	chr5:118517397-118517398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555950237	chr5:118517423-118517424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184218909	chr5:118517430-118517431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569755145	chr5:118517431-118517432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189634841	chr5:118517450-118517451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577762908	chr5:118517459-118517460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540239811	chr5:118517486-118517487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181852379	chr5:118517490-118517491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529207662	chr5:118517491-118517492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186103503	chr5:118517530-118517531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374477684	chr5:118517532-118517533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4382194	chr5:118517540-118517541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4257802	chr5:118517543-118517544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148588728	chr5:118517561-118517562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189348009	chr5:118517592-118517593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550708240	chr5:118517631-118517632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114589847	chr5:118517645-118517646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371029852	chr5:118517682-118517683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114021998	chr5:118517686-118517687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546605123	chr5:118517695-118517696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181449223	chr5:118517697-118517698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536175574	chr5:118517741-118517742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151042674	chr5:118517776-118517777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575837272	chr5:118517800-118517801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538054488	chr5:118517803-118517804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187032275	chr5:118517813-118517814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558339491	chr5:118517842-118517843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20531469	CNVD

Chromatin state (count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118412200-118522800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr5:118451200-118533400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:118453800-118522800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr5:118479000-118526000	Weak transcription	Fetal Brain Male	brain
5	chr5:118483000-118541400	Weak transcription	NHEK	skin
6	chr5:118485400-118522800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr5:118485800-118534000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:118485800-118572200	Weak transcription	Small Intestine	intestine
9	chr5:118486000-118534200	Weak transcription	Brain Angular Gyrus	brain
10	chr5:118486000-118588600	Weak transcription	Right Ventricle	heart
11	chr5:118486200-118526000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:118486200-118534200	Weak transcription	Colon Smooth Muscle	Colon
13	chr5:118489800-118591200	Weak transcription	Colonic Mucosa	Colon
14	chr5:118490800-118526000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr5:118490800-118526200	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr5:118490800-118532000	Weak transcription	Brain Hippocampus Middle	brain
17	chr5:118491200-118532400	Weak transcription	Fetal Kidney	kidney
18	chr5:118493400-118528000	Weak transcription	Fetal Brain Female	brain
19	chr5:118494600-118534600	Weak transcription	Psoas Muscle	Psoas
20	chr5:118497200-118532800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:118497800-118534400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:118497800-118535200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:118498000-118534400	Weak transcription	Lung	lung
24	chr5:118498000-118584200	Weak transcription	Spleen	Spleen
25	chr5:118499800-118534400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:118501800-118519200	Weak transcription	Fetal Intestine Small	intestine
27	chr5:118501800-118519200	Weak transcription	Fetal Stomach	stomach
28	chr5:118501800-118520400	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr5:118501800-118524000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:118501800-118526000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr5:118501800-118533000	Weak transcription	Left Ventricle	heart
32	chr5:118501800-118533800	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr5:118501800-118533800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:118502000-118528600	Weak transcription	Fetal Thymus	thymus
35	chr5:118502400-118525200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr5:118503800-118585800	Weak transcription	NH-A	brain
37	chr5:118504200-118522400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr5:118504600-118522200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr5:118504600-118522400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr5:118504600-118522800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr5:118504600-118532600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr5:118504800-118518800	Weak transcription	HUVEC	blood vessel
43	chr5:118504800-118522400	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr5:118504800-118533400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:118505400-118554600	Weak transcription	HepG2	liver
46	chr5:118507000-118522200	Weak transcription	Primary T cells from cord blood	blood
47	chr5:118507000-118533400	Weak transcription	HSMMtube	muscle
48	chr5:118507800-118580200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr5:118510000-118519200	Weak transcription	Fetal Muscle Trunk	muscle
50	chr5:118510000-118526000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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