Variant report

Variant	nsv887603
Chromosome Location	chr7:11104985-11231727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:0)
Chromatin interactive
region (count:71)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:11122472-11122755	HepG2	liver:	n/a	n/a
2	ATF1	chr7:11221045-11221594	K562	blood:	n/a	n/a
3	ATF1	chr7:11128773-11128831	K562	blood:	n/a	n/a
4	ATF2	chr7:11224807-11225248	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:11122404-11123057	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:11224855-11225204	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:11175371-11175473	K562	blood:	n/a	n/a
8	BACH1	chr7:11231364-11231607	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr7:11118139-11118345	GM12878	blood:	n/a	chr7:11118255-11118265
10	BATF	chr7:11160374-11160600	GM12878	blood:	n/a	n/a
11	BATF	chr7:11118081-11118314	GM12878	blood:	n/a	chr7:11118255-11118265
12	BCL11A	chr7:11224826-11225121	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr7:11224931-11225119	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr7:11195043-11195271	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:11215693-11215816	K562	blood:	n/a	n/a
16	BHLHE40	chr7:11210726-11210891	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:11228287-11228806	K562	blood:	n/a	n/a
18	BRCA1	chr7:11167087-11167179	GM12878	blood:	n/a	n/a
19	CCNT2	chr7:11217186-11217420	K562	blood:	n/a	n/a
20	CEBPB	chr7:11210526-11210841	IMR90	lung:	n/a	chr7:11210690-11210701
21	CEBPB	chr7:11122652-11122903	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:11210550-11210871	HepG2	liver:	n/a	chr7:11210690-11210701
23	CEBPB	chr7:11124748-11125014	K562	blood:	n/a	chr7:11124881-11124894
24	CEBPB	chr7:11115589-11115882	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:11210530-11210811	Hela-S3	cervix:	n/a	chr7:11210690-11210701
26	CEBPB	chr7:11108217-11108264	H1-hESC	embryonic stem cell:	n/a	chr7:11108241-11108252
27	CEBPB	chr7:11108099-11108373	A549	lung:	n/a	chr7:11108241-11108252
28	CEBPB	chr7:11115591-11115952	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:11108137-11108367	K562	blood:	n/a	chr7:11108241-11108252
30	CEBPB	chr7:11115581-11115979	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:11124794-11124970	HepG2	liver:	n/a	chr7:11124881-11124894
32	CEBPB	chr7:11115591-11115931	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:11169609-11170090	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:11115586-11115929	A549	lung:	n/a	n/a
35	CEBPB	chr7:11115583-11115943	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:11224751-11225301	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:11108116-11108371	HepG2	liver:	n/a	chr7:11108241-11108252
38	CEBPB	chr7:11210548-11210824	A549	lung:	n/a	chr7:11210690-11210701
39	CEBPB	chr7:11115611-11115936	K562	blood:	n/a	n/a
40	CEBPB	chr7:11122659-11123159	A549	lung:	n/a	n/a
41	CHD2	chr7:11224770-11225237	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr7:11210819-11211347	GM12878	blood:	n/a	n/a
43	CREB1	chr7:11160285-11160708	GM12878	blood:	n/a	n/a
44	CREB1	chr7:11221129-11221613	K562	blood:	n/a	n/a
45	CTCF	chr7:11205503-11205565	GM10248	blood:	n/a	chr7:11205529-11205550
46	CTCF	chr7:11193420-11193570	AG09319	gingival:	n/a	n/a
47	CTCF	chr7:11205503-11205584	GM10266	blood:	n/a	chr7:11205529-11205550
48	CTCF	chr7:11169973-11169981	K562	blood:	n/a	n/a
49	CTCF	chr7:11193420-11193570	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr7:11110120-11110270	BJ	skin:	n/a	n/a

No data

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:11179754..11182412-chr7:11187476..11189973,2	K562	blood:
2	chr7:11192916..11193961-chr7:11251567..11252421,4	MCF-7	breast:
3	chr7:11187936..11191247-chr7:11191383..11194500,4	K562	blood:
4	chr7:11140028..11142682-chr7:11145035..11147597,3	K562	blood:
5	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
6	chr7:11136221..11139675-chr7:11144358..11148872,4	K562	blood:
7	chr7:11113760..11116450-chr7:11117895..11120001,2	MCF-7	breast:
8	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
9	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
10	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
11	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
12	chr7:11140028..11142682-chr7:11145035..11146787,2	K562	blood:
13	chr7:11120505..11122093-chr7:11122139..11123895,2	K562	blood:
14	chr7:11130768..11133783-chr7:11134322..11137393,4	K562	blood:
15	chr7:11193379..11193920-chr7:11380707..11381612,2	MCF-7	breast:
16	chr7:11197789..11199466-chr7:11199534..11202480,2	K562	blood:
17	chr7:11175308..11177163-chr7:11367863..11369367,2	MCF-7	breast:
18	chr7:11196790..11199292-chr7:11202946..11205439,2	K562	blood:
19	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
20	chr7:11230694..11232235-chr7:11241525..11243997,2	MCF-7	breast:
21	chr7:11022666..11024973-chr7:11118639..11120820,2	K562	blood:
22	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
23	chr7:11193091..11193870-chr7:11383205..11383845,2	MCF-7	breast:
24	chr7:11166607..11168180-chr7:11168609..11170188,2	MCF-7	breast:
25	chr7:11193309..11193972-chr7:11380975..11381751,3	MCF-7	breast:
26	chr7:11121943..11123973-chr7:11130475..11132999,2	K562	blood:
27	chr7:11169416..11171057-chr7:11171117..11173550,2	K562	blood:
28	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
29	chr7:11120505..11122093-chr7:11122139..11123895,2	K562	blood:
30	chr7:11102318..11104655-chr7:11104749..11107010,2	K562	blood:
31	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
32	chr7:11121943..11123973-chr7:11130475..11132999,2	K562	blood:
33	chr7:11146142..11148658-chr7:11151256..11153162,2	K562	blood:
34	chr7:11162615..11164289-chr7:11165693..11168328,2	K562	blood:
35	chr7:11012606..11015240-chr7:11166727..11169294,2	MCF-7	breast:
36	chr7:11141298..11142996-chr7:11151745..11153861,2	MCF-7	breast:
37	chr7:11108681..11111650-chr7:11117427..11119548,2	K562	blood:
38	chr7:11229782..11232630-chr7:11260914..11263136,3	K562	blood:
39	chr7:11104144..11105857-chr7:11109203..11110826,2	K562	blood:
40	chr7:11088216..11090960-chr7:11126210..11129188,2	K562	blood:
41	chr7:11126725..11129133-chr7:11132639..11135110,2	MCF-7	breast:
42	chr17:78500461..78501088-chr7:11221500..11222496,2	HCT-116	colon:
43	chr7:11121527..11123973-chr7:11131499..11134132,2	K562	blood:
44	chr7:11196790..11199546-chr7:11202946..11205522,2	K562	blood:
45	chr7:11118440..11120387-chr7:11122259..11124478,2	K562	blood:
46	chr7:11197217..11199466-chr7:11200911..11202480,2	K562	blood:
47	chr7:11124384..11127270-chr7:11131542..11136731,4	K562	blood:
48	chr7:11141677..11144293-chr7:11222755..11224742,2	K562	blood:
49	chr7:11130768..11133331-chr7:11134322..11136010,2	K562	blood:
50	chr7:11205391..11208108-chr7:11211440..11214054,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-1	chr7:11228166-11228261	ENSG00000230333.2
2	lnc-PHF14-1	chr7:11221359-11221463	ENSG00000230333.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF14	hsa-miR-155-5p	chr7:11148709-11148731
2	PHF14	hsa-miR-155-5p	chr7:11142813-11142835
3	PHF14	hsa-miR-155-5p	chr7:11142799-11142820

Variant related genes	Relation type
PHF14	TF binding region
ENSG00000230333	TF binding region
ENSG00000106443	chromatin interactions
ENSG00000196204	chromatin interactions

Extended variants
information (count: 5132 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5132 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs721028	chr7:11104985-11104986	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79887248	chr7:11105005-11105006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531947401	chr7:11105031-11105032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116353275	chr7:11105037-11105038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2883141	chr7:11105060-11105061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562216599	chr7:11105087-11105088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569372069	chr7:11105097-11105098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538720513	chr7:11105099-11105100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188046806	chr7:11105165-11105166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560887265	chr7:11105169-11105170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558416599	chr7:11105202-11105203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141332027	chr7:11105245-11105246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201033449	chr7:11105251-11105252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180766912	chr7:11105264-11105265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566614965	chr7:11105287-11105288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184612855	chr7:11105343-11105344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529717936	chr7:11105348-11105349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551915794	chr7:11105368-11105369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568818078	chr7:11105369-11105370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374593297	chr7:11105428-11105429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10240831	chr7:11105452-11105453	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533811816	chr7:11105454-11105455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566529937	chr7:11105590-11105591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532385713	chr7:11105611-11105612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554867459	chr7:11105637-11105638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567964268	chr7:11105643-11105644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190343363	chr7:11105670-11105671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182590764	chr7:11105751-11105752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545869286	chr7:11105815-11105816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186545146	chr7:11105817-11105818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576407706	chr7:11105855-11105856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs80048234	chr7:11105864-11105865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190664547	chr7:11105884-11105885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs118023399	chr7:11105895-11105896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541694872	chr7:11105919-11105920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564650664	chr7:11105935-11105936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115253699	chr7:11105939-11105940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552262346	chr7:11105940-11105941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568828957	chr7:11105958-11105959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531338531	chr7:11105959-11105960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76958051	chr7:11105966-11105967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568054929	chr7:11105980-11105981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181127546	chr7:11105991-11105992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150334643	chr7:11106000-11106001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570329546	chr7:11106005-11106006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75450917	chr7:11106012-11106013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56208661	chr7:11106024-11106025	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs80014362	chr7:11106057-11106058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555797886	chr7:11106111-11106112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185779766	chr7:11106149-11106150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD

Chromatin state (count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11014800-11117400	Weak transcription	HSMMtube	muscle
2	chr7:11015200-11108200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr7:11035800-11113000	Weak transcription	Esophagus	oesophagus
4	chr7:11035800-11113200	Weak transcription	Lung	lung
5	chr7:11035800-11123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:11039000-11108800	Weak transcription	Psoas Muscle	Psoas
7	chr7:11046000-11128600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr7:11046200-11175000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr7:11046600-11122600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:11046600-11167800	Weak transcription	Thymus	Thymus
11	chr7:11048200-11113400	Weak transcription	Aorta	Aorta
12	chr7:11054400-11113200	Weak transcription	Pancreas	Pancrea
13	chr7:11057800-11190200	Weak transcription	Fetal Brain Male	brain
14	chr7:11064400-11112400	Weak transcription	Brain Germinal Matrix	brain
15	chr7:11064400-11112400	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:11064400-11122800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr7:11064600-11111800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:11066400-11106800	Weak transcription	Fetal Kidney	kidney
19	chr7:11071800-11113000	Weak transcription	Fetal Intestine Small	intestine
20	chr7:11071800-11113000	Weak transcription	Fetal Stomach	stomach
21	chr7:11076400-11193200	Weak transcription	Ovary	ovary
22	chr7:11076800-11122200	Weak transcription	HMEC	breast
23	chr7:11077000-11130600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:11077000-11162400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr7:11077200-11108800	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:11077600-11106400	Weak transcription	NH-A	brain
27	chr7:11078600-11122400	Weak transcription	Fetal Muscle Leg	muscle
28	chr7:11078800-11116200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr7:11079200-11111600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:11086600-11143800	Weak transcription	HUVEC	blood vessel
31	chr7:11090600-11107400	Strong transcription	Dnd41	blood
32	chr7:11091000-11116400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr7:11091800-11174200	Weak transcription	Left Ventricle	heart
34	chr7:11092600-11112600	Weak transcription	Fetal Brain Female	brain
35	chr7:11092600-11122400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:11092600-11122600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:11092800-11106800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr7:11094200-11122000	Weak transcription	HepG2	liver
39	chr7:11094600-11153400	Weak transcription	Hela-S3	cervix
40	chr7:11095600-11122800	Weak transcription	Brain Anterior Caudate	brain
41	chr7:11097400-11129000	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr7:11098400-11122000	Weak transcription	A549	lung
43	chr7:11099400-11111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr7:11099800-11128800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:11101200-11105800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:11101800-11109800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:11102200-11109400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:11102200-11112200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr7:11102200-11126200	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr7:11102200-11189200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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