Variant report

Variant	nsv608376
Chromosome Location	chr7:126457779-126571077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:126509086-126509186	K562	blood:	n/a	n/a
2	ATF1	chr7:126489638-126489672	K562	blood:	n/a	n/a
3	BATF	chr7:126551713-126552013	GM12878	blood:	n/a	chr7:126551879-126551890
4	BCL11A	chr7:126522058-126522240	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:126496848-126496879	HepG2	liver:	n/a	n/a
6	CCNT2	chr7:126473119-126473313	K562	blood:	n/a	n/a
7	CEBPB	chr7:126522805-126523396	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:126513084-126513338	HepG2	liver:	n/a	chr7:126513180-126513191
9	CEBPB	chr7:126459081-126459332	HepG2	liver:	n/a	chr7:126459237-126459248 chr7:126459239-126459250 chr7:126459237-126459250
10	CEBPB	chr7:126524473-126524687	K562	blood:	n/a	chr7:126524616-126524628 chr7:126524579-126524592 chr7:126524579-126524590
11	CEBPB	chr7:126524451-126524692	Hela-S3	cervix:	n/a	chr7:126524616-126524628 chr7:126524579-126524592 chr7:126524579-126524590
12	CEBPB	chr7:126526182-126526382	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:126516526-126516933	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr7:126512782-126513296	A549	lung:	n/a	chr7:126513180-126513191 chr7:126513051-126513062
15	CEBPB	chr7:126524439-126524641	HepG2	liver:	n/a	chr7:126524616-126524628 chr7:126524579-126524592 chr7:126524579-126524590
16	CTCF	chr7:126496771-126497046	Medullo	brain:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
17	CTCF	chr7:126540180-126540330	Caco-2	colon:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
18	CTCF	chr7:126496773-126497047	MCF-7	breast:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
19	CTCF	chr7:126541341-126541365	Gliobla	brain:	n/a	n/a
20	CTCF	chr7:126527889-126527945	GM10248	blood:	n/a	n/a
21	CTCF	chr7:126540118-126540380	GM12878	blood:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
22	CTCF	chr7:126522142-126522244	Medullo	brain:	n/a	n/a
23	CTCF	chr7:126521917-126522360	A549	lung:	n/a	n/a
24	CTCF	chr7:126496860-126497010	GM12864	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
25	CTCF	chr7:126540559-126540577	GM12878	blood:	n/a	n/a
26	CTCF	chr7:126496840-126496990	HBMEC	blood vessel:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
27	CTCF	chr7:126496880-126497030	GM12878	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
28	CTCF	chr7:126540220-126540370	HBMEC	blood vessel:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
29	CTCF	chr7:126540240-126540390	NHDF-neo	bronchial:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
30	CTCF	chr7:126540147-126540350	A549	lung:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
31	CTCF	chr7:126540300-126540450	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr7:126496840-126496990	K562	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
33	CTCF	chr7:126540260-126540410	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr7:126539740-126539890	BE2_C	brain:	n/a	n/a
35	CTCF	chr7:126540097-126540392	LNCaP	prostate:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
36	CTCF	chr7:126540240-126540390	WERI-Rb-1	eye:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
37	CTCF	chr7:126540158-126540387	GM10248	blood:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
38	CTCF	chr7:126540260-126540410	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr7:126496822-126497015	Kidney_OC	kidney:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
40	CTCF	chr7:126540122-126540361	GM19238	blood:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
41	CTCF	chr7:126540020-126540170	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr7:126496860-126497010	GM12874	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
43	CTCF	chr7:126496840-126496990	HEEpiC	esophagus:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
44	CTCF	chr7:126496835-126497009	GM13976	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
45	CTCF	chr7:126540240-126540390	GM12872	blood:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
46	CTCF	chr7:126540240-126540390	HRPEpiC	eye:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
47	CTCF	chr7:126522095-126522264	GM10248	blood:	n/a	n/a
48	CTCF	chr7:126540140-126540290	WERI-Rb-1	eye:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
49	CTCF	chr7:126496753-126497068	IMR90	lung:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
50	CTCF	chr7:126522069-126522257	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126483492..126485257-chr7:126496192..126497874,2	K562	blood:
2	7:126477235-126483531..7:127070190-127076279	Hela-S3	cervix:
3	7:126537894-126544517..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
4	chr7:126492682..126494185-chr7:126494985..126497035,2	K562	blood:
5	chr7:126496786..126498746-chr7:126500529..126502173,2	MCF-7	breast:
6	chr7:126492682..126494185-chr7:126494985..126497035,2	K562	blood:
7	7:126477235-126483531..7:126746034-126750148	H1-hESC	embryonic stem cell:	embryo
8	chr7:126477944..126479476-chr7:126481551..126483101,2	K562	blood:
9	chr7:126496786..126498746-chr7:126500529..126502173,2	MCF-7	breast:
10	7:126474837-126476627..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
11	7:126470017-126471969..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
12	chr7:126443207..126444075-chr7:126540061..126540769,2	MCF-7	breast:
13	7:126477235-126483531..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
14	chr7:126483492..126485257-chr7:126496192..126497874,2	K562	blood:
15	7:126085913-126088095..7:126492401-126497300	GM12878	blood:
16	7:126085913-126088095..7:126563918-126569249	K562	blood:
17	chr7:126477944..126479476-chr7:126481551..126483101,2	K562	blood:
18	7:126085913-126088095..7:126537894-126544517	GM12878	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF800-7	chr7:126508821-126510586	NONHSAT123122

Variant related genes	Relation type
ENSG00000224981	TF binding region
ENSG00000048405	chromatin interactions
ENSG00000179603	chromatin interactions

Extended variants
information (count: 2201 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534084433	chr7:126458809-126458810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192698649	chr7:126458885-126458886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574488243	chr7:126458895-126458896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541890493	chr7:126458943-126458944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556564770	chr7:126458971-126458972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574864096	chr7:126458980-126458981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12706747	chr7:126458996-126458997	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs534081902	chr7:126459061-126459062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564000469	chr7:126459074-126459075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528294364	chr7:126459090-126459091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141581468	chr7:126459112-126459113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553050293	chr7:126459126-126459127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573230024	chr7:126459130-126459131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540104961	chr7:126459177-126459178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150195702	chr7:126459233-126459234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561914719	chr7:126459292-126459293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369112717	chr7:126459317-126459318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372499463	chr7:126459321-126459322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113435220	chr7:126459329-126459330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs3038867	chr7:126459351-126459352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74450114	chr7:126459352-126459353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79180407	chr7:126459353-126459354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74925926	chr7:126459354-126459355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185597847	chr7:126459359-126459360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551072822	chr7:126459360-126459361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560305158	chr7:126461025-126461026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527648848	chr7:126461066-126461067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139032375	chr7:126461157-126461158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144169744	chr7:126461169-126461170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373345337	chr7:126461196-126461197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146512544	chr7:126461203-126461204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571494430	chr7:126461216-126461217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192139831	chr7:126461298-126461299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181823372	chr7:126461420-126461421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139933038	chr7:126461429-126461430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143399702	chr7:126461436-126461437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555378382	chr7:126461449-126461450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574022762	chr7:126461455-126461456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541544748	chr7:126461462-126461463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146715540	chr7:126461472-126461473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556420351	chr7:126461526-126461527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563418548	chr7:126461527-126461528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149165836	chr7:126461551-126461552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73451295	chr7:126461564-126461565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143288490	chr7:126461574-126461575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371382480	chr7:126461608-126461609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572350285	chr7:126461668-126461669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543056943	chr7:126461757-126461758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577659916	chr7:126461763-126461764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141924474	chr7:126461766-126461767	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Autism	22495311	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
Metanephric adenoma	20802469	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
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126458800-126459400	Enhancers	Liver	Liver
2	chr7:126461000-126461800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:126463000-126463200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:126471400-126471800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
5	chr7:126471400-126473600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:126482600-126484400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:126483000-126484200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr7:126484400-126487200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:126485200-126486000	Enhancers	HUVEC	blood vessel
10	chr7:126487200-126488400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:126492000-126492200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr7:126492200-126493200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr7:126493200-126495000	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr7:126493800-126494200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:126494200-126496600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:126495800-126496000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:126496600-126497000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:126496600-126497400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:126496600-126497400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:126496600-126497400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:126496800-126497400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr7:126496800-126498600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:126497000-126497400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:126497000-126497400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:126497000-126497400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:126497000-126497800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr7:126497400-126498400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr7:126497400-126498600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr7:126497400-126498600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr7:126497400-126498600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr7:126498600-126498800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:126498600-126498800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:126498800-126499000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:126498800-126499000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr7:126498800-126499000	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:126508200-126508400	Enhancers	Pancreas	Pancrea
37	chr7:126513600-126513800	Enhancers	Small Intestine	intestine
38	chr7:126516200-126517000	Enhancers	Hela-S3	cervix
39	chr7:126517000-126521400	Weak transcription	Hela-S3	cervix
40	chr7:126521400-126521600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr7:126521400-126521800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:126521400-126521800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr7:126521400-126521800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:126521400-126521800	Enhancers	Lung	lung
45	chr7:126521400-126521800	Enhancers	Hela-S3	cervix
46	chr7:126521600-126521800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr7:126521800-126523000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr7:126521800-126523000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr7:126521800-126523000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr7:126521800-126523200	Weak transcription	Hela-S3	cervix

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