Variant report

Variant	nsv981680
Chromosome Location	chr7:128288269-128298277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:367)
Chromatin interactive
region (count:0)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr7:128291764-128292046	K562	blood:	n/a	n/a
2	CBX3	chr7:128293288-128293860	K562	blood:	n/a	n/a
3	CEBPB	chr7:128293555-128293810	K562	blood:	n/a	n/a
4	CEBPB	chr7:128293514-128293858	K562	blood:	n/a	n/a
5	CTCF	chr7:128293320-128293470	A549	lung:	n/a	n/a
6	CTCF	chr7:128291860-128292010	GM12873	blood:	n/a	n/a
7	CTCF	chr7:128291896-128291980	GM12878	blood:	n/a	n/a
8	CTCF	chr7:128295200-128295350	GM12866	blood:	n/a	n/a
9	CTCF	chr7:128291860-128292010	NB4	blood:	n/a	n/a
10	CTCF	chr7:128291880-128292030	GM12871	blood:	n/a	n/a
11	CTCF	chr7:128291880-128292030	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr7:128291880-128292030	NHEK	skin:	n/a	n/a
13	CTCF	chr7:128290760-128290910	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr7:128291880-128292030	AG04449	skin:	n/a	n/a
15	CTCF	chr7:128291530-128292073	K562	blood:	n/a	n/a
16	CTCF	chr7:128293220-128293370	HepG2	liver:	n/a	n/a
17	CTCF	chr7:128290498-128290876	K562	blood:	n/a	n/a
18	CTCF	chr7:128293380-128293530	MCF-7	breast:	n/a	n/a
19	CTCF	chr7:128291840-128291990	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr7:128293320-128293470	GM12868	blood:	n/a	n/a
21	CTCF	chr7:128291900-128292050	SAEC	small airway:	n/a	n/a
22	CTCF	chr7:128291424-128292223	K562	blood:	n/a	n/a
23	CTCF	chr7:128291880-128292030	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr7:128291938-128291953	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:128291900-128292050	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:128295344-128295412	H1-hESC	embryonic stem cell:	n/a	chr7:128295374-128295387
27	CTCF	chr7:128291840-128291990	GM12873	blood:	n/a	n/a
28	CTCF	chr7:128291907-128291988	Gliobla	brain:	n/a	n/a
29	CTCF	chr7:128295220-128295370	HepG2	liver:	n/a	n/a
30	CTCF	chr7:128291840-128291990	SAEC	small airway:	n/a	n/a
31	CTCF	chr7:128291880-128292030	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:128295220-128295370	RPTEC	kidney:	n/a	n/a
33	CTCF	chr7:128295177-128295636	K562	blood:	n/a	chr7:128295374-128295387
34	CTCF	chr7:128291840-128291990	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:128295220-128295370	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:128291892-128292030	K562	blood:	n/a	n/a
37	CTCF	chr7:128295200-128295350	HCT-116	colon:	n/a	n/a
38	CTCF	chr7:128291920-128292070	HMEC	breast:	n/a	n/a
39	CTCF	chr7:128293360-128293510	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:128291900-128292050	GM12866	blood:	n/a	n/a
41	CTCF	chr7:128293220-128293370	SAEC	small airway:	n/a	n/a
42	CTCF	chr7:128293211-128293584	K562	blood:	n/a	n/a
43	CTCF	chr7:128291913-128291985	GM12878	blood:	n/a	n/a
44	CTCF	chr7:128291880-128292030	RPTEC	kidney:	n/a	n/a
45	CTCF	chr7:128291810-128292061	K562	blood:	n/a	n/a
46	CTCF	chr7:128291840-128291990	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr7:128291840-128291990	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr7:128295280-128295430	WERI-Rb-1	eye:	n/a	chr7:128295374-128295387
49	CTCF	chr7:128295197-128295563	K562	blood:	n/a	chr7:128295374-128295387
50	CTCF	chr7:128291840-128291990	AG09319	gingival:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128293588-128293638	K562	blood:	n/a
2	chr7:128293588-128293638	K562	blood:	n/a
3	chr7:128292968-128293018	Jurkat	blood:	n/a
4	chr7:128294794-128294844	NB4	blood:	n/a
5	chr7:128293588-128293638	AG04450	lung:	fetal
6	chr7:128294794-128294844	MCF10A-Er-Src	breast:	n/a
7	chr7:128293588-128293638	Jurkat	blood:	n/a
8	chr7:128294794-128294844	K562	blood:	n/a
9	chr7:128294794-128294844	AG04449	skin:	fetal
10	chr7:128294405-128294455	HepG2	liver:	n/a
11	chr7:128294794-128294844	IMR90	lung:	fetal
12	chr7:128293756-128293806	LNCaP	prostate:	n/a
13	chr7:128292968-128293018	SK-N-MC	brain:	n/a
14	chr7:128293588-128293638	NT2-D1	testis:	n/a
15	chr7:128294794-128294844	U87	brain:	n/a
16	chr7:128293756-128293806	GM12891	blood:	n/a
17	chr7:128294405-128294455	T-47D	breast:	n/a
18	chr7:128294405-128294455	HCM	heart:	n/a
19	chr7:128294794-128294844	PANC-1	pancreas:	n/a
20	chr7:128292968-128293018	HIPEpiC	eye:	n/a
21	chr7:128293588-128293638	T-47D	breast:	n/a
22	chr7:128294083-128294133	HMEC	breast:	n/a
23	chr7:128294405-128294455	Jurkat	blood:	n/a
24	chr7:128293588-128293638	ProgFib	skin:	n/a
25	chr7:128294083-128294133	A549	lung:	n/a
26	chr7:128294083-128294133	LNCaP	prostate:	n/a
27	chr7:128293588-128293638	IMR90	lung:	fetal
28	chr7:128293756-128293806	NHDF-neo	bronchial:	n/a
29	chr7:128292968-128293018	AG09309	skin:	n/a
30	chr7:128292968-128293018	AG10803	skin:	n/a
31	chr7:128293756-128293806	Jurkat	blood:	n/a
32	chr7:128294405-128294455	SK-N-SH	brain:	n/a
33	chr7:128293756-128293806	HAEpiC	amniotic membrane:	n/a
34	chr7:128293756-128293806	GM19239	blood:	n/a
35	chr7:128294794-128294844	HNPCEpiC	eye:	n/a
36	chr7:128292968-128293018	Hepatocyte	liver:	n/a
37	chr7:128294083-128294133	HEK293	kidney:	embryo
38	chr7:128293756-128293806	HIPEpiC	eye:	n/a
39	chr7:128294083-128294133	AG04450	lung:	fetal
40	chr7:128293756-128293806	HRE	kidney:	n/a
41	chr7:128293588-128293638	LNCaP	prostate:	n/a
42	chr7:128293756-128293806	BJ	skin:	n/a
43	chr7:128293756-128293806	MCF-7	breast:	n/a
44	chr7:128292968-128293018	HepG2	liver:	n/a
45	chr7:128294083-128294133	HCPEpiC	choroid plexus:	n/a
46	chr7:128294083-128294133	HCM	heart:	n/a
47	chr7:128292968-128293018	PFSK-1	brain:	n/a
48	chr7:128292968-128293018	SK-N-SH_RA	brain:	n/a
49	chr7:128294794-128294844	HIPEpiC	eye:	n/a
50	chr7:128294405-128294455	HEK293	kidney:	embryo

No data

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71F2-1	chr7:128288846-128289036	NONHSAT123222
2	lnc-FAM71F2-1	chr7:128291239-128292388	NONHSAT123224
3	lnc-FAM71F2-1	chr7:128288960-128289038	NONHSAT123221
4	lnc-FAM71F2-1	chr7:128288846-128288927	NONHSAT123221
5	lnc-FAM71F2-1	chr7:128291092-128291134	NONHSAT123222
6	lnc-FAM71F2-1	chr7:128288846-128289174	NONHSAT123218
7	lnc-FAM71F2-1	chr7:128291243-128291452	NONHSAT123221
8	lnc-FAM71F2-1	chr7:128288840-128289065	NONHSAT123217
9	lnc-FAM71F2-1	chr7:128291092-128291151	NONHSAT123221

No data

Variant related genes	Relation type
ENSG00000243679	TF binding region
ENSG00000229413	TF binding region
ENSG00000230715	TF binding region
ENSG00000243302	TF binding region
ENSG00000243679	CpG island
ENSG00000229413	CpG island
ENSG00000230715	CpG island
ENSG00000243302	CpG island

Extended variants
information (count: 350 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57122781	chr7:128288320-128288321	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs60915147	chr7:128288363-128288364	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs9691920	chr7:128288374-128288375	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs374059820	chr7:128288387-128288388	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs568304029	chr7:128288459-128288460	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs12154232	chr7:128288497-128288498	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs535734707	chr7:128288508-128288509	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs10954196	chr7:128288591-128288592	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs12056197	chr7:128288627-128288628	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs10954197	chr7:128288633-128288634	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs556902648	chr7:128288654-128288655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12056198	chr7:128288670-128288671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148953998	chr7:128288730-128288731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
14	rs539553211	chr7:128288731-128288732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10954198	chr7:128288741-128288742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112011701	chr7:128288802-128288803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112960487	chr7:128288803-128288804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10954199	chr7:128288853-128288854	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs557841019	chr7:128288886-128288887	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs113277178	chr7:128288908-128288909	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs113055348	chr7:128288909-128288910	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs12056217	chr7:128289002-128289003	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs71546790	chr7:128289004-128289005	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs539891113	chr7:128289008-128289009	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs555338648	chr7:128289022-128289023	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs10954200	chr7:128289031-128289032	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs10954201	chr7:128289036-128289037	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs12056223	chr7:128289057-128289058	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs12056224	chr7:128289068-128289069	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs574281010	chr7:128289088-128289089	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs62481909	chr7:128289128-128289129	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs12056004	chr7:128289209-128289210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12056225	chr7:128289286-128289287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113519581	chr7:128289659-128289660	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs374101123	chr7:128289667-128289668	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs62481910	chr7:128289811-128289812	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
37	rs201241786	chr7:128289851-128289852	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
38	rs12055939	chr7:128289873-128289874	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
39	rs12055941	chr7:128290013-128290014	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs12056251	chr7:128290100-128290101	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
41	rs10954202	chr7:128290110-128290111	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
42	rs573285139	chr7:128290158-128290159	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
43	rs12056029	chr7:128290171-128290172	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
44	rs200749313	chr7:128290203-128290204	Weak transcription Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
45	rs12056257	chr7:128290214-128290215	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs12154726	chr7:128290229-128290230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12155370	chr7:128290244-128290245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12155374	chr7:128290264-128290265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111254711	chr7:128290323-128290324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10954203	chr7:128290402-128290403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128237800-128290400	Weak transcription	HepG2	liver
2	chr7:128239200-128296400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:128242600-128292800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:128249600-128289000	Weak transcription	NHEK	skin
5	chr7:128249600-128293400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr7:128249600-128295200	Weak transcription	NH-A	brain
7	chr7:128249600-128297600	Weak transcription	HUVEC	blood vessel
8	chr7:128249600-128308400	Weak transcription	HSMM	muscle
9	chr7:128249600-128312200	Weak transcription	Psoas Muscle	Psoas
10	chr7:128249600-128319600	Weak transcription	NHLF	lung
11	chr7:128256800-128288600	Weak transcription	Osteobl	bone
12	chr7:128260000-128296400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr7:128260400-128300600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:128262200-128293200	Weak transcription	Brain Germinal Matrix	brain
15	chr7:128265800-128289000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:128266400-128290400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr7:128272200-128300000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:128272400-128290400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr7:128272400-128290400	Weak transcription	K562	blood
20	chr7:128272400-128292400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr7:128272400-128293200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:128273600-128290600	Weak transcription	Fetal Brain Female	brain
23	chr7:128273800-128291800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr7:128274200-128296400	Weak transcription	Colonic Mucosa	Colon
25	chr7:128274600-128291200	Weak transcription	Esophagus	oesophagus
26	chr7:128275600-128295000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:128275800-128289600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:128278000-128289000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:128278400-128289000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:128279600-128296200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr7:128279800-128291200	Weak transcription	Gastric	stomach
32	chr7:128279800-128291800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr7:128279800-128292600	Weak transcription	Aorta	Aorta
34	chr7:128279800-128292600	Weak transcription	Brain Substantia Nigra	brain
35	chr7:128279800-128293000	Weak transcription	Rectal Smooth Muscle	rectum
36	chr7:128279800-128293600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr7:128279800-128296400	Weak transcription	Brain Angular Gyrus	brain
38	chr7:128279800-128300000	Weak transcription	Dnd41	blood
39	chr7:128279800-128301400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr7:128280400-128291000	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr7:128280400-128291800	Weak transcription	Right Ventricle	heart
42	chr7:128281200-128293200	Weak transcription	Ovary	ovary
43	chr7:128281400-128291200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr7:128281400-128291800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr7:128281400-128292400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr7:128281600-128290600	Weak transcription	Pancreas	Pancrea
47	chr7:128281600-128290800	Weak transcription	Brain Anterior Caudate	brain
48	chr7:128281600-128291800	Weak transcription	Brain Hippocampus Middle	brain
49	chr7:128281800-128291400	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr7:128282200-128291400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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