Variant report

Variant	nsv470001
Chromosome Location	chr4:2680515-2723531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:624)
CpG islands
(count:306)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:2697995-2698718	GM12878	blood:	n/a	n/a
2	ATF2	chr4:2693689-2694309	GM12878	blood:	n/a	n/a
3	ATF2	chr4:2697871-2698708	GM12878	blood:	n/a	n/a
4	ATF3	chr4:2691673-2691891	GM12878	blood:	n/a	n/a
5	BATF	chr4:2714153-2714433	GM12878	blood:	n/a	n/a
6	BATF	chr4:2698084-2698552	GM12878	blood:	n/a	n/a
7	BATF	chr4:2691670-2691928	GM12878	blood:	n/a	n/a
8	BATF	chr4:2714241-2714436	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:2693791-2694131	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:2698095-2698489	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:2698041-2698507	GM12878	blood:	n/a	n/a
12	BCLAF1	chr4:2698033-2698657	GM12878	blood:	n/a	n/a
13	BCLAF1	chr4:2697963-2698880	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:2713889-2714317	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:2693915-2694205	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:2691521-2692259	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:2699808-2700120	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:2698003-2698670	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:2714283-2714392	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:2693799-2694411	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:2696495-2696661	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:2716278-2716614	GM12878	blood:	n/a	n/a
23	CEBPB	chr4:2716695-2716951	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:2698119-2698462	GM12878	blood:	n/a	n/a
25	CEBPB	chr4:2699827-2699925	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:2704978-2705137	K562	blood:	n/a	n/a
27	CEBPB	chr4:2697949-2698638	GM12878	blood:	n/a	n/a
28	CEBPB	chr4:2709418-2709570	K562	blood:	n/a	n/a
29	CEBPB	chr4:2704972-2705080	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:2704957-2705088	IMR90	lung:	n/a	n/a
31	CHD1	chr4:2691596-2691673	GM12878	blood:	n/a	n/a
32	CHD1	chr4:2687250-2687986	IMR90	lung:	n/a	n/a
33	CHD1	chr4:2694201-2694214	GM12878	blood:	n/a	n/a
34	CHD2	chr4:2691681-2691974	GM12878	blood:	n/a	n/a
35	CHD2	chr4:2693891-2694296	GM12878	blood:	n/a	n/a
36	CHD2	chr4:2698061-2698723	GM12878	blood:	n/a	n/a
37	CREB1	chr4:2698013-2698652	GM12878	blood:	n/a	n/a
38	CTCF	chr4:2715740-2715890	AG04450	lung:	n/a	n/a
39	CTCF	chr4:2698240-2698390	GM06990	blood:	n/a	chr4:2698338-2698351
40	CTCF	chr4:2698280-2698430	GM06990	blood:	n/a	chr4:2698338-2698351
41	CTCF	chr4:2713898-2714291	MCF-7	breast:	n/a	n/a
42	CTCF	chr4:2714120-2714270	GM06990	blood:	n/a	n/a
43	CTCF	chr4:2698400-2698550	GM12870	blood:	n/a	n/a
44	CTCF	chr4:2698380-2698530	GM12866	blood:	n/a	n/a
45	CTCF	chr4:2714100-2714250	AG04449	skin:	n/a	n/a
46	CTCF	chr4:2715780-2715930	NHLF	lung:	n/a	n/a
47	CTCF	chr4:2714120-2714270	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr4:2714089-2714267	IMR90	lung:	n/a	n/a
49	CTCF	chr4:2723300-2723450	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr4:2714040-2714190	HUVEC	blood vessel:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2696786-2696836	HAEpiC	amniotic membrane:	n/a
2	chr4:2696786-2696836	HAEpiC	amniotic membrane:	n/a
3	chr4:2696631-2696681	PANC-1	pancreas:	n/a
4	chr4:2687547-2687597	NH-A	brain:	n/a
5	chr4:2696786-2696836	BE2_C	brain:	n/a
6	chr4:2696715-2696765	HMEC	breast:	n/a
7	chr4:2696631-2696681	LNCaP	prostate:	n/a
8	chr4:2696786-2696836	HRCEpiC	kidney:	n/a
9	chr4:2716524-2716574	A549	lung:	n/a
10	chr4:2696631-2696681	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:2716524-2716574	NT2-D1	testis:	n/a
12	chr4:2687547-2687597	HRCEpiC	kidney:	n/a
13	chr4:2696786-2696836	NB4	blood:	n/a
14	chr4:2687547-2687597	LNCaP	prostate:	n/a
15	chr4:2687547-2687597	T-47D	breast:	n/a
16	chr4:2696631-2696681	NT2-D1	testis:	n/a
17	chr4:2696786-2696836	H1-hESC	embryonic stem cell:	embryo
18	chr4:2696715-2696765	HCM	heart:	n/a
19	chr4:2696631-2696681	ProgFib	skin:	n/a
20	chr4:2696631-2696681	Hepatocyte	liver:	n/a
21	chr4:2687547-2687597	SK-N-MC	brain:	n/a
22	chr4:2696631-2696681	HCPEpiC	choroid plexus:	n/a
23	chr4:2687547-2687597	NHBE	bronchial:	n/a
24	chr4:2716524-2716574	BJ	skin:	n/a
25	chr4:2687547-2687597	Hela-S3	cervix:	n/a
26	chr4:2696786-2696836	HEK293	kidney:	embryo
27	chr4:2696786-2696836	Jurkat	blood:	n/a
28	chr4:2696715-2696765	HIPEpiC	eye:	n/a
29	chr4:2696786-2696836	PANC-1	pancreas:	n/a
30	chr4:2696715-2696765	AG04450	lung:	fetal
31	chr4:2687547-2687597	AoSMC	blood vessel:	n/a
32	chr4:2716524-2716574	LNCaP	prostate:	n/a
33	chr4:2696786-2696836	Hela-S3	cervix:	n/a
34	chr4:2696631-2696681	GM12878	blood:	n/a
35	chr4:2696786-2696836	T-47D	breast:	n/a
36	chr4:2696786-2696836	HIPEpiC	eye:	n/a
37	chr4:2696631-2696681	SKMC	muscle:	n/a
38	chr4:2696631-2696681	HRCEpiC	kidney:	n/a
39	chr4:2696715-2696765	GM12878	blood:	n/a
40	chr4:2687547-2687597	SKMC	muscle:	n/a
41	chr4:2696786-2696836	NT2-D1	testis:	n/a
42	chr4:2696631-2696681	HIPEpiC	eye:	n/a
43	chr4:2716524-2716574	NHDF-neo	bronchial:	n/a
44	chr4:2687547-2687597	A549	lung:	n/a
45	chr4:2696715-2696765	HRE	kidney:	n/a
46	chr4:2696715-2696765	Hepatocyte	liver:	n/a
47	chr4:2716524-2716574	AG09319	gingival:	n/a
48	chr4:2696631-2696681	AG04450	lung:	fetal
49	chr4:2716524-2716574	NB4	blood:	n/a
50	chr4:2687547-2687597	K562	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:2709028..2711083-chr4:2714281..2716848,2	K562	blood:
2	chr4:2694438..2696914-chr4:2698682..2700465,2	K562	blood:
3	chr4:2671638..2673716-chr4:2684803..2686606,2	MCF-7	breast:
4	chr4:2693061..2695542-chr4:2698679..2700261,2	K562	blood:
5	chr4:2686800..2688519-chr4:2692243..2694641,2	MCF-7	breast:
6	chr4:2698027..2699882-chr4:2708019..2712089,3	K562	blood:
7	chr4:2684900..2686631-chr4:2732347..2735002,2	MCF-7	breast:
8	chr4:2686800..2688519-chr4:2692243..2694641,2	MCF-7	breast:
9	chr4:2698027..2699882-chr4:2708019..2712089,3	K562	blood:
10	chr4:2536163..2539003-chr4:2712977..2717563,4	MCF-7	breast:
11	chr4:2536351..2537886-chr4:2713685..2715325,2	MCF-7	breast:
12	chr4:2686405..2688173-chr4:2690940..2692757,2	K562	blood:
13	chr4:2694438..2696914-chr4:2698682..2700465,2	K562	blood:
14	chr4:2714914..2717325-chr4:2756410..2757959,2	MCF-7	breast:
15	chr4:2693061..2695542-chr4:2698679..2700261,2	K562	blood:
16	chr4:2681997..2685012-chr4:2686552..2689862,4	K562	blood:
17	chr11:62608625..62609221-chr4:2723288..2724083,2	NB4	blood:
18	chr4:2691900..2694094-chr4:2704691..2707252,2	MCF-7	breast:
19	chr4:2681997..2685012-chr4:2686552..2689862,4	K562	blood:
20	chr4:2709028..2711083-chr4:2714281..2716848,2	K562	blood:
21	chr4:2691900..2694094-chr4:2704691..2707252,2	MCF-7	breast:
22	chr4:2673139..2674929-chr4:2692013..2693790,2	K562	blood:
23	chr4:2687414..2693444-chr4:2695682..2700044,5	MCF-7	breast:
24	chr4:2686405..2688173-chr4:2690940..2692757,2	K562	blood:
25	chr4:2722338..2725244-chr4:2727735..2730949,3	K562	blood:

No data

Variant related genes	Relation type
FAM193A	TF binding region
FAM193A	CpG island
ENSG00000125386	chromatin interactions
ENSG00000168884	chromatin interactions

Extended variants
information (count: 1936 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1936 , 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	rs7681728	chr4:2680515-2680516	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79705497	chr4:2680518-2680519	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576394969	chr4:2680520-2680521	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4040735	chr4:2680527-2680528	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543096562	chr4:2680551-2680552	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373552955	chr4:2680563-2680564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562117768	chr4:2680568-2680569	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548313257	chr4:2680597-2680598	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527799113	chr4:2680613-2680614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541430438	chr4:2680624-2680625	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531347681	chr4:2680753-2680754	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533647844	chr4:2680758-2680759	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188050698	chr4:2680803-2680804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368014550	chr4:2680805-2680806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576730693	chr4:2680860-2680861	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570267106	chr4:2680870-2680871	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529458513	chr4:2680893-2680894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549310902	chr4:2680914-2680915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116755409	chr4:2680940-2680941	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372484432	chr4:2681002-2681003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193093743	chr4:2681017-2681018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143525027	chr4:2681021-2681022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59543318	chr4:2681034-2681035	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs58230072	chr4:2681084-2681085	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs183688602	chr4:2681085-2681086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs202109350	chr4:2681094-2681095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371052372	chr4:2681098-2681099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369296261	chr4:2681102-2681103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201754447	chr4:2681104-2681105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57578410	chr4:2681105-2681106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113268337	chr4:2681106-2681107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs56038080	chr4:2681158-2681159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576261013	chr4:2681200-2681201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541968108	chr4:2681260-2681261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555643145	chr4:2681312-2681313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542010678	chr4:2681325-2681326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543600341	chr4:2681333-2681334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138603727	chr4:2681340-2681341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148032858	chr4:2681341-2681342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376720085	chr4:2681351-2681352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568178901	chr4:2681352-2681353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564459436	chr4:2681357-2681358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577932433	chr4:2681358-2681359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543472508	chr4:2681359-2681360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563957133	chr4:2681373-2681374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201265336	chr4:2681397-2681398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529570061	chr4:2681403-2681404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549156751	chr4:2681421-2681422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559565070	chr4:2681500-2681501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188204487	chr4:2681532-2681533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Facial dysmorphism	22438245	CNVD
Wolf-Hirschhorn syndrome	22438245	CNVD
Breast cancer	22522925	CNVD
Cancer	22970210	CNVD
Disease	21248748	CNVD
Gastric cancer	21784958	CNVD
Systemic lupus erythematosus	22942739	CNVD

Chromatin state (count:1237 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2627200-2683600	Strong transcription	Fetal Thymus	thymus
2	chr4:2638200-2724400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:2662600-2685600	Weak transcription	Fetal Brain Male	brain
4	chr4:2669600-2692200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr4:2671200-2682400	Strong transcription	Liver	Liver
6	chr4:2673600-2714400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:2673800-2698000	Weak transcription	Fetal Heart	heart
8	chr4:2674200-2682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:2674200-2685600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:2674200-2686400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:2674200-2695600	Weak transcription	Stomach Mucosa	stomach
12	chr4:2674600-2685600	Weak transcription	Brain Substantia Nigra	brain
13	chr4:2674800-2681800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:2674800-2683200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:2674800-2685800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr4:2674800-2685800	Weak transcription	HMEC	breast
17	chr4:2674800-2686400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr4:2675200-2682000	Weak transcription	Spleen	Spleen
19	chr4:2675200-2683200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr4:2675200-2685200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr4:2675200-2685800	Weak transcription	Pancreas	Pancrea
22	chr4:2675200-2685800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr4:2675200-2691600	Weak transcription	Small Intestine	intestine
24	chr4:2675200-2698200	Weak transcription	Psoas Muscle	Psoas
25	chr4:2675400-2685400	Weak transcription	HSMMtube	muscle
26	chr4:2675400-2685800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr4:2675400-2689200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr4:2675600-2686200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr4:2675600-2692000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr4:2676000-2685600	Weak transcription	Colon Smooth Muscle	Colon
31	chr4:2676200-2684400	Weak transcription	HUVEC	blood vessel
32	chr4:2676200-2685600	Weak transcription	Brain Germinal Matrix	brain
33	chr4:2676200-2685600	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr4:2676400-2685600	Weak transcription	Aorta	Aorta
35	chr4:2676400-2685600	Weak transcription	Lung	lung
36	chr4:2676400-2685600	Weak transcription	Right Ventricle	heart
37	chr4:2676400-2685800	Weak transcription	Esophagus	oesophagus
38	chr4:2676400-2685800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr4:2676400-2686200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr4:2676600-2685600	Weak transcription	Brain Anterior Caudate	brain
41	chr4:2677000-2685600	Weak transcription	Fetal Brain Female	brain
42	chr4:2677000-2685600	Weak transcription	Fetal Kidney	kidney
43	chr4:2677200-2682000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr4:2677200-2685600	Weak transcription	Brain Angular Gyrus	brain
45	chr4:2677200-2685600	Weak transcription	Left Ventricle	heart
46	chr4:2677200-2685600	Weak transcription	NH-A	brain
47	chr4:2677200-2685800	Weak transcription	Ovary	ovary
48	chr4:2677200-2692200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr4:2677400-2682200	Weak transcription	Fetal Muscle Trunk	muscle
50	chr4:2677400-2685600	Weak transcription	Thymus	Thymus

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