Variant report

Variant	nsv966883
Chromosome Location	chr7:128107081-128142581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1088)
CpG islands
(count:854)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:128116656-128116994	HepG2	liver:	n/a	chr7:128116722-128116737
2	ARID3A	chr7:128116683-128116924	K562	blood:	n/a	chr7:128116722-128116737
3	ATF1	chr7:128116429-128116963	K562	blood:	n/a	n/a
4	ATF2	chr7:128116648-128116919	GM12878	blood:	n/a	n/a
5	ATF2	chr7:128116502-128117079	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:128116459-128117089	GM12878	blood:	n/a	n/a
7	ATF3	chr7:128116574-128117018	A549	lung:	n/a	n/a
8	BATF	chr7:128116594-128116950	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:128116868-128117161	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:128116536-128116824	GM12878	blood:	n/a	chr7:128116670-128116678 chr7:128116654-128116663
11	BCL3	chr7:128116351-128117099	A549	lung:	n/a	chr7:128116670-128116678 chr7:128116654-128116663
12	BCL3	chr7:128116371-128117099	A549	lung:	n/a	chr7:128116670-128116678 chr7:128116654-128116663
13	BCLAF1	chr7:128116430-128117083	GM12878	blood:	n/a	chr7:128116670-128116678 chr7:128116654-128116663
14	BCLAF1	chr7:128116477-128117088	K562	blood:	n/a	chr7:128116670-128116678 chr7:128116654-128116663
15	BCLAF1	chr7:128116544-128117095	K562	blood:	n/a	chr7:128116670-128116678 chr7:128116654-128116663
16	BHLHE40	chr7:128117454-128117501	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:128117409-128117617	K562	blood:	n/a	n/a
18	BHLHE40	chr7:128116657-128116989	K562	blood:	n/a	n/a
19	BHLHE40	chr7:128116716-128116952	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:128116560-128116989	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr7:128116602-128116960	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr7:128116638-128116989	GM12878	blood:	n/a	n/a
23	BRCA1	chr7:128116673-128116940	HepG2	liver:	n/a	n/a
24	CBX3	chr7:128116351-128117049	K562	blood:	n/a	n/a
25	CBX3	chr7:128116163-128117737	K562	blood:	n/a	n/a
26	CCNT2	chr7:128116683-128116971	K562	blood:	n/a	n/a
27	CEBPB	chr7:128116577-128117393	GM12878	blood:	n/a	n/a
28	CEBPB	chr7:128116661-128116963	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:128116622-128116974	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:128116230-128117133	K562	blood:	n/a	n/a
31	CEBPB	chr7:128116626-128116956	A549	lung:	n/a	n/a
32	CEBPB	chr7:128122084-128122351	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr7:128116656-128116992	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:128116661-128116956	K562	blood:	n/a	n/a
35	CEBPB	chr7:128116611-128117038	Hela-S3	cervix:	n/a	n/a
36	CEBPD	chr7:128116419-128117095	K562	blood:	n/a	n/a
37	CEBPD	chr7:128116655-128116973	HepG2	liver:	n/a	n/a
38	CHD1	chr7:128117255-128117257	GM12878	blood:	n/a	n/a
39	CHD2	chr7:128116576-128117033	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr7:128116499-128117095	K562	blood:	n/a	n/a
41	CHD2	chr7:128116568-128117041	HepG2	liver:	n/a	n/a
42	CHD2	chr7:128116504-128117080	GM12878	blood:	n/a	n/a
43	CHD2	chr7:128116474-128117119	Hela-S3	cervix:	n/a	n/a
44	CREB1	chr7:128116572-128116909	A549	lung:	n/a	n/a
45	CREB1	chr7:128116485-128117079	A549	lung:	n/a	n/a
46	CREB1	chr7:128116576-128116858	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr7:128116780-128116930	SAEC	small airway:	n/a	n/a
48	CTCF	chr7:128114300-128114450	AG09309	skin:	n/a	n/a
49	CTCF	chr7:128114320-128114470	AG04450	lung:	n/a	n/a
50	CTCF	chr7:128109693-128109946	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128116967-128117017	LNCaP	prostate:	n/a
2	chr7:128120649-128120699	GM19239	blood:	n/a
3	chr7:128114609-128114659	HAEpiC	amniotic membrane:	n/a
4	chr7:128116644-128116694	HAEpiC	amniotic membrane:	n/a
5	chr7:128116967-128117017	PANC-1	pancreas:	n/a
6	chr7:128116668-128116718	NHBE	bronchial:	n/a
7	chr7:128117206-128117256	PFSK-1	brain:	n/a
8	chr7:128116967-128117017	GM12878	blood:	n/a
9	chr7:128117206-128117256	BJ	skin:	n/a
10	chr7:128116561-128116611	NT2-D1	testis:	n/a
11	chr7:128120649-128120699	PANC-1	pancreas:	n/a
12	chr7:128116644-128116694	RPTEC	kidney:	n/a
13	chr7:128116813-128116863	HNPCEpiC	eye:	n/a
14	chr7:128116782-128116832	SKMC	muscle:	n/a
15	chr7:128116412-128116462	NHDF-neo	bronchial:	n/a
16	chr7:128116561-128116611	HIPEpiC	eye:	n/a
17	chr7:128116589-128116639	HEEpiC	esophagus:	n/a
18	chr7:128116813-128116863	SKMC	muscle:	n/a
19	chr7:128116782-128116832	GM06990	blood:	n/a
20	chr7:128116782-128116832	HIPEpiC	eye:	n/a
21	chr7:128114609-128114659	PFSK-1	brain:	n/a
22	chr7:128116644-128116694	NB4	blood:	n/a
23	chr7:128116782-128116832	SK-N-MC	brain:	n/a
24	chr7:128116813-128116863	GM12891	blood:	n/a
25	chr7:128116412-128116462	GM12878	blood:	n/a
26	chr7:128116813-128116863	T-47D	breast:	n/a
27	chr7:128116967-128117017	NHDF-neo	bronchial:	n/a
28	chr7:128116561-128116611	AG09319	gingival:	n/a
29	chr7:128116807-128116857	AG09319	gingival:	n/a
30	chr7:128117206-128117256	GM12878	blood:	n/a
31	chr7:128117206-128117256	AG09309	skin:	n/a
32	chr7:128120649-128120699	SK-N-SH_RA	brain:	n/a
33	chr7:128116807-128116857	H1-hESC	embryonic stem cell:	embryo
34	chr7:128116807-128116857	AoSMC	blood vessel:	n/a
35	chr7:128116589-128116639	GM12892	blood:	n/a
36	chr7:128116732-128116782	CMK	blood:	n/a
37	chr7:128116967-128117017	ECC-1	luminal epithelium:	n/a
38	chr7:128116561-128116611	HCT-116	colon:	n/a
39	chr7:128117206-128117256	PANC-1	pancreas:	n/a
40	chr7:128116668-128116718	HRE	kidney:	n/a
41	chr7:128114609-128114659	Hepatocyte	liver:	n/a
42	chr7:128117206-128117256	HCF	heart:	n/a
43	chr7:128116561-128116611	HCPEpiC	choroid plexus:	n/a
44	chr7:128114609-128114659	SK-N-SH_RA	brain:	n/a
45	chr7:128120649-128120699	HCT-116	colon:	n/a
46	chr7:128120649-128120699	H1-hESC	embryonic stem cell:	embryo
47	chr7:128117206-128117256	HEEpiC	esophagus:	n/a
48	chr7:128116412-128116462	HRPEpiC	eye:	n/a
49	chr7:128117206-128117256	HAEpiC	amniotic membrane:	n/a
50	chr7:128116732-128116782	HEEpiC	esophagus:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:16118309..16118871-chr7:128116620..128117465,2	Hela-S3	cervix:
2	chr7:128139215..128142117-chr7:128174144..128176717,2	K562	blood:
3	chr7:128117849..128119350-chr7:128175808..128177783,2	K562	blood:
4	chr7:128095158..128096724-chr7:128104393..128107346,2	K562	blood:
5	chr7:128116092..128118343-chr7:128171049..128172892,4	K562	blood:
6	chr7:128115485..128120196-chr7:128120953..128124102,5	MCF-7	breast:
7	chr7:128116465..128119803-chr7:128169321..128173196,4	MCF-7	breast:
8	chr7:128115173..128117389-chr7:128298817..128301721,2	K562	blood:
9	chr7:128140732..128143190-chr7:128377049..128379381,2	K562	blood:
10	chr7:128121751..128124643-chr7:128170477..128172903,2	K562	blood:
11	chr7:128049014..128051472-chr7:128115731..128117859,3	K562	blood:
12	chr7:128095923..128097516-chr7:128115288..128116864,2	K562	blood:
13	chr7:128139891..128142505-chr7:128169322..128171236,2	MCF-7	breast:
14	chr7:128094286..128097516-chr7:128115288..128118444,4	K562	blood:
15	chr14:35008396..35009205-chr7:128116073..128116780,2	Hela-S3	cervix:
16	chr17:60500926..60501465-chr7:128116355..128117240,2	NB4	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HILPDA-1	chr7:128120701-128120750	ENSG00000273184.1
2	lnc-HILPDA-1	chr7:128119212-128119567	ENSG00000273184.1
3	lnc-HILPDA-1	chr7:128128155-128128215	ENSG00000273184.1
4	lnc-HILPDA-1	chr7:128133858-128133913	ENSG00000273184.1

No data

Variant related genes	Relation type
METTL2B	TF binding region
METTL2B	CpG island
ENSG00000087995	chromatin interactions
ENSG00000129518	chromatin interactions
ENSG00000128595	chromatin interactions
ENSG00000271529	chromatin interactions
ENSG00000273184	chromatin interactions
ENSG00000242588	chromatin interactions
ENSG00000240758	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000135245	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000273270	chromatin interactions
ENSG00000165055	chromatin interactions

Extended variants
information (count: 1381 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1381 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558616989	chr7:128107145-128107146	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs2732403	chr7:128107160-128107161	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs574413218	chr7:128107169-128107170	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs541929429	chr7:128107202-128107203	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs563092260	chr7:128107206-128107207	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs530538310	chr7:128107241-128107242	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs3110278	chr7:128107309-128107310	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs3110279	chr7:128107314-128107315	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs147582001	chr7:128107335-128107336	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs62481129	chr7:128107355-128107356	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528642854	chr7:128107402-128107403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199961777	chr7:128107460-128107461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533592462	chr7:128107472-128107473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62481130	chr7:128107475-128107476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546826991	chr7:128107506-128107507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71160651	chr7:128107511-128107512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568655712	chr7:128107515-128107516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149060872	chr7:128107698-128107699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192033847	chr7:128107701-128107702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569144795	chr7:128107702-128107703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181702249	chr7:128107707-128107708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537635686	chr7:128107819-128107820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186760085	chr7:128107824-128107825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377753807	chr7:128107841-128107842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs55924291	chr7:128107868-128107869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574579540	chr7:128107869-128107870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541521770	chr7:128107878-128107879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554472350	chr7:128107881-128107882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557059755	chr7:128107885-128107886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182389031	chr7:128107887-128107888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545425972	chr7:128107913-128107914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185131034	chr7:128107939-128107940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573167796	chr7:128107980-128107981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116435731	chr7:128108011-128108012	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs202224680	chr7:128108027-128108028	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540548673	chr7:128108032-128108033	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372215664	chr7:128108047-128108048	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562098035	chr7:128108056-128108057	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529528479	chr7:128108071-128108072	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550791581	chr7:128108103-128108104	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563025229	chr7:128108105-128108106	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189595477	chr7:128108156-128108157	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551763652	chr7:128108184-128108185	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566893697	chr7:128108185-128108186	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201917654	chr7:128108187-128108188	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183370635	chr7:128108188-128108189	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188712170	chr7:128108225-128108226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549080433	chr7:128108309-128108310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374705150	chr7:128108311-128108312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141070254	chr7:128108315-128108316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	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	chr7:128096400-128116400	Weak transcription	Lung	lung
2	chr7:128097400-128107800	Weak transcription	Spleen	Spleen
3	chr7:128097600-128116200	Weak transcription	Fetal Kidney	kidney
4	chr7:128097600-128116200	Weak transcription	Left Ventricle	heart
5	chr7:128097800-128116400	Weak transcription	Fetal Stomach	stomach
6	chr7:128097800-128116400	Weak transcription	Gastric	stomach
7	chr7:128097800-128116400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:128098200-128116400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:128098200-128116400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:128098400-128108000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:128098600-128116200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:128098800-128108200	Weak transcription	Fetal Muscle Leg	muscle
13	chr7:128099000-128116200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr7:128099000-128116400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr7:128099200-128116400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr7:128099400-128116200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr7:128099400-128116400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr7:128099800-128116200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr7:128099800-128116200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr7:128099800-128116400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr7:128099800-128116400	Weak transcription	Fetal Intestine Small	intestine
22	chr7:128099800-128116400	Weak transcription	Ovary	ovary
23	chr7:128100000-128108000	Weak transcription	Fetal Brain Female	brain
24	chr7:128100000-128109000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr7:128100000-128116200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:128100000-128116200	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr7:128100000-128116200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:128100000-128116400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:128100000-128116400	Weak transcription	Brain Hippocampus Middle	brain
30	chr7:128100000-128116400	Weak transcription	Esophagus	oesophagus
31	chr7:128100000-128116400	Weak transcription	Fetal Brain Male	brain
32	chr7:128100200-128108000	Weak transcription	Brain Anterior Caudate	brain
33	chr7:128100200-128108000	Weak transcription	Dnd41	blood
34	chr7:128100200-128116200	Weak transcription	Brain Germinal Matrix	brain
35	chr7:128100200-128116200	Weak transcription	K562	blood
36	chr7:128100400-128108200	Weak transcription	Adipose Nuclei	Adipose
37	chr7:128100400-128116200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr7:128100600-128116200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr7:128102800-128116200	Weak transcription	A549	lung
40	chr7:128103000-128116200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr7:128103000-128116200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr7:128103000-128116200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr7:128103000-128116200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:128103000-128116200	Weak transcription	Fetal Heart	heart
45	chr7:128103000-128116200	Weak transcription	NHLF	lung
46	chr7:128103200-128109800	Weak transcription	Right Ventricle	heart
47	chr7:128103600-128116200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr7:128103800-128108000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:128103800-128108000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:128103800-128116400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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