Variant report

Variant	nsv525319
Chromosome Location	chr7:127929271-127946173
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:127939408-127939596	K562	blood:	n/a	n/a
2	BHLHE40	chr7:127938259-127938392	HepG2	liver:	n/a	n/a
3	CBX3	chr7:127931568-127932076	K562	blood:	n/a	n/a
4	CBX3	chr7:127931732-127932059	K562	blood:	n/a	n/a
5	CEBPB	chr7:127930403-127930544	K562	blood:	n/a	chr7:127930525-127930536
6	CEBPB	chr7:127945691-127945856	A549	lung:	n/a	n/a
7	CEBPB	chr7:127930523-127930538	IMR90	lung:	n/a	chr7:127930525-127930536
8	CEBPB	chr7:127930433-127930580	HepG2	liver:	n/a	chr7:127930525-127930536
9	CHD2	chr7:127939860-127939937	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F4	chr7:127945326-127945481	MCF10A-Er-Src	breast:	n/a	n/a
11	EP300	chr7:127938103-127938425	HepG2	liver:	n/a	n/a
12	FOXA1	chr7:127938029-127938377	HepG2	liver:	n/a	n/a
13	FOXA1	chr7:127932323-127932684	HepG2	liver:	n/a	n/a
14	FOXA2	chr7:127932146-127932867	A549	lung:	n/a	n/a
15	FOXA2	chr7:127932430-127932839	A549	lung:	n/a	n/a
16	GTF2F1	chr7:127939373-127939502	H1-hESC	embryonic stem cell:	n/a	n/a
17	GTF2F1	chr7:127939886-127939928	H1-hESC	embryonic stem cell:	n/a	n/a
18	HNF4A	chr7:127938172-127938410	HepG2	liver:	n/a	chr7:127938273-127938288 chr7:127938307-127938322
19	HNF4A	chr7:127938092-127938414	HepG2	liver:	n/a	chr7:127938273-127938288 chr7:127938307-127938322
20	KAP1	chr7:127931723-127932060	K562	blood:	n/a	n/a
21	MAFK	chr7:127944221-127944473	HepG2	liver:	n/a	n/a
22	MAFK	chr7:127944287-127944437	HepG2	liver:	n/a	n/a
23	MAX	chr7:127939987-127940170	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAX	chr7:127939158-127939580	H1-hESC	embryonic stem cell:	n/a	n/a
25	MYC	chr7:127939340-127939760	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr7:127941045-127942024	PFSK-1	brain:	n/a	n/a
27	POLR2A	chr7:127941472-127941925	PANC-1	pancreas:	n/a	n/a
28	POLR2A	chr7:127944444-127944976	K562	blood:	n/a	n/a
29	POLR2A	chr7:127940943-127941287	K562	blood:	n/a	n/a
30	POLR2A	chr7:127940138-127940195	K562	blood:	n/a	n/a
31	POLR2A	chr7:127944512-127944639	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:127941389-127942183	U87	brain:	n/a	n/a
33	POLR2A	chr7:127945512-127946419	K562	blood:	n/a	n/a
34	POLR2A	chr7:127942399-127942423	K562	blood:	n/a	n/a
35	POLR2A	chr7:127942741-127943167	K562	blood:	n/a	n/a
36	POLR2A	chr7:127941480-127942063	A549	lung:	n/a	n/a
37	POLR2A	chr7:127941433-127941546	HepG2	liver:	n/a	n/a
38	POLR2A	chr7:127940663-127940703	K562	blood:	n/a	n/a
39	POLR2A	chr7:127943462-127943666	HepG2	liver:	n/a	n/a
40	POLR2A	chr7:127942898-127942903	K562	blood:	n/a	n/a
41	POLR2A	chr7:127941335-127942107	K562	blood:	n/a	n/a
42	POLR2A	chr7:127945168-127946823	K562	blood:	n/a	n/a
43	POLR2A	chr7:127940029-127942189	SK-N-MC	brain:	n/a	n/a
44	POLR2A	chr7:127943332-127943922	K562	blood:	n/a	n/a
45	POLR2A	chr7:127940846-127940919	K562	blood:	n/a	n/a
46	POLR2A	chr7:127944344-127944700	K562	blood:	n/a	n/a
47	POLR2A	chr7:127945508-127946971	K562	blood:	n/a	n/a
48	POLR2A	chr7:127941573-127941575	HepG2	liver:	n/a	n/a
49	POLR2A	chr7:127945793-127945834	HepG2	liver:	n/a	n/a
50	POLR2A	chr7:127945547-127945956	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127940559-127940609	H1-hESC	embryonic stem cell:	embryo
2	chr7:127940559-127940609	SKMC	muscle:	n/a
3	chr7:127940559-127940609	GM06990	blood:	n/a
4	chr7:127940559-127940609	GM19239	blood:	n/a
5	chr7:127940559-127940609	HCPEpiC	choroid plexus:	n/a
6	chr7:127940559-127940609	SK-N-SH_RA	brain:	n/a
7	chr7:127940559-127940609	HMEC	breast:	n/a
8	chr7:127940559-127940609	AG09309	skin:	n/a
9	chr7:127940559-127940609	PANC-1	pancreas:	n/a
10	chr7:127940559-127940609	GM12891	blood:	n/a
11	chr7:127940559-127940609	AG04450	lung:	fetal
12	chr7:127940559-127940609	CMK	blood:	n/a
13	chr7:127940559-127940609	U87	brain:	n/a
14	chr7:127940559-127940609	HCM	heart:	n/a
15	chr7:127940559-127940609	T-47D	breast:	n/a
16	chr7:127940559-127940609	HRE	kidney:	n/a
17	chr7:127940559-127940609	MCF10A-Er-Src	breast:	n/a
18	chr7:127940559-127940609	NB4	blood:	n/a
19	chr7:127940559-127940609	Hela-S3	cervix:	n/a
20	chr7:127940559-127940609	HAEpiC	amniotic membrane:	n/a
21	chr7:127940559-127940609	AG09319	gingival:	n/a
22	chr7:127940559-127940609	AG04449	skin:	fetal
23	chr7:127940559-127940609	HL-60	blood:	n/a
24	chr7:127940559-127940609	Caco-2	colon:	n/a
25	chr7:127940559-127940609	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:127940559-127940609	K562	blood:	n/a
27	chr7:127940559-127940609	AoSMC	blood vessel:	n/a
28	chr7:127940559-127940609	SK-N-SH	brain:	n/a
29	chr7:127940559-127940609	HEEpiC	esophagus:	n/a
30	chr7:127940559-127940609	BJ	skin:	n/a
31	chr7:127940559-127940609	ProgFib	skin:	n/a
32	chr7:127940559-127940609	SK-N-MC	brain:	n/a
33	chr7:127940559-127940609	LNCaP	prostate:	n/a
34	chr7:127940559-127940609	GM12878	blood:	n/a
35	chr7:127940559-127940609	Jurkat	blood:	n/a
36	chr7:127940559-127940609	PFSK-1	brain:	n/a
37	chr7:127940559-127940609	IMR90	lung:	fetal
38	chr7:127940559-127940609	ECC-1	luminal epithelium:	n/a
39	chr7:127940559-127940609	BE2_C	brain:	n/a
40	chr7:127940559-127940609	HepG2	liver:	n/a
41	chr7:127940559-127940609	NT2-D1	testis:	n/a
42	chr7:127940559-127940609	HCT-116	colon:	n/a
43	chr7:127940559-127940609	GM12892	blood:	n/a
44	chr7:127940559-127940609	HUVEC	blood vessel:	n/a
45	chr7:127940559-127940609	A549	lung:	n/a
46	chr7:127940559-127940609	HIPEpiC	eye:	n/a
47	chr7:127940559-127940609	PrEC	prostate:	n/a
48	chr7:127940559-127940609	Hepatocyte	liver:	n/a
49	chr7:127940559-127940609	MCF-7	breast:	n/a
50	chr7:127940559-127940609	SAEC	small airway:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:127937053..127939817-chr7:127940949..127943521,2	K562	blood:
2	chr7:127940019..127941640-chr7:127955342..127957765,2	K562	blood:
3	chr7:127941056..127943858-chr7:127948197..127950566,3	K562	blood:
4	chr7:127938979..127940740-chr7:127949044..127951138,2	K562	blood:
5	chr7:127940010..127942133-chr7:127944769..127947134,2	MCF-7	breast:
6	chr7:127940674..127942545-chr7:127948588..127950322,2	MCF-7	breast:
7	chr7:127937053..127939817-chr7:127940949..127943521,2	K562	blood:
8	chr7:127940151..127942923-chr7:127964464..127966540,2	MCF-7	breast:
9	chr7:127941056..127943858-chr7:127948197..127950137,2	K562	blood:
10	chr7:127940082..127943532-chr7:127944561..127947795,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM28-1	chr7:127930781-127931619	NONHSAT123176
2	lnc-RBM28-3	chr7:127937738-127947816	NONHSAT123178
3	lnc-RBM28-3	chr7:127944240-127946359	NONHSAT123179

No data

Variant related genes	Relation type
ENSG00000221429	TF binding region
ENSG00000242261	TF binding region
ENSG00000221429	CpG island
ENSG00000242261	CpG island
ENSG00000242261	chromatin interactions

Extended variants
information (count: 610 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17618714	chr7:127929271-127929272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376985301	chr7:127929328-127929329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200810450	chr7:127929331-127929332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201794017	chr7:127929334-127929335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200327255	chr7:127929335-127929336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201586208	chr7:127929336-127929337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs199534073	chr7:127929337-127929338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200354733	chr7:127929338-127929339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73228306	chr7:127929341-127929342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs34594421	chr7:127929454-127929455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531167658	chr7:127929523-127929524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73456868	chr7:127929537-127929538	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548199347	chr7:127929555-127929556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111574076	chr7:127929556-127929557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546991049	chr7:127929563-127929564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143549905	chr7:127929578-127929579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536526305	chr7:127929581-127929582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527352121	chr7:127929611-127929612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554614768	chr7:127929612-127929613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569506528	chr7:127929631-127929632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62666460	chr7:127929680-127929681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375590934	chr7:127929726-127929727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147501206	chr7:127929738-127929739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs55881232	chr7:127929743-127929744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191202722	chr7:127929768-127929769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570523828	chr7:127929776-127929777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148562902	chr7:127929792-127929793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552910363	chr7:127929842-127929843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183929616	chr7:127929860-127929861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542496617	chr7:127929884-127929885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115982063	chr7:127929885-127929886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531083044	chr7:127929920-127929921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116310485	chr7:127929986-127929987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564541280	chr7:127929997-127929998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188935017	chr7:127930029-127930030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546808081	chr7:127930060-127930061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569603170	chr7:127930062-127930063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6943621	chr7:127930084-127930085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191637870	chr7:127930102-127930103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574885297	chr7:127930133-127930134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375574721	chr7:127930158-127930159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534001827	chr7:127930195-127930196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151115918	chr7:127930196-127930197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536815462	chr7:127930217-127930218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570072289	chr7:127930218-127930219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570339833	chr7:127930273-127930274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140031839	chr7:127930287-127930288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372920561	chr7:127930349-127930350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371583074	chr7:127930427-127930428	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs10251133	chr7:127930441-127930442	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:76)

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
small cell lung cancer	20016488	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127917000-127945600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:127917200-127943200	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr7:127920200-127945200	Weak transcription	Right Ventricle	heart
4	chr7:127920600-127938800	Weak transcription	Right Atrium	heart
5	chr7:127920600-127941000	Weak transcription	Primary T cells from cord blood	blood
6	chr7:127920800-127931000	Weak transcription	Fetal Lung	lung
7	chr7:127921400-127939000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr7:127921800-127944400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:127922000-127940600	Weak transcription	Brain Anterior Caudate	brain
10	chr7:127922000-127942000	Weak transcription	Brain Angular Gyrus	brain
11	chr7:127922000-127944400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr7:127922200-127930800	Weak transcription	Brain Germinal Matrix	brain
13	chr7:127922200-127932600	Weak transcription	Fetal Intestine Small	intestine
14	chr7:127922200-127942000	Weak transcription	Left Ventricle	heart
15	chr7:127922200-127942200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr7:127922200-127943000	Weak transcription	Dnd41	blood
17	chr7:127922200-127943200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr7:127922400-127932000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:127922400-127942000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:127923800-127943200	Weak transcription	Pancreas	Pancrea
21	chr7:127924000-127940000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr7:127924200-127943800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr7:127924400-127942200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:127924400-127942200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr7:127924600-127939000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:127924600-127940600	Weak transcription	A549	lung
27	chr7:127924600-127950000	Weak transcription	Psoas Muscle	Psoas
28	chr7:127926200-127940200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:127926400-127930600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:127926400-127943200	Weak transcription	HSMM	muscle
31	chr7:127926600-127930400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:127926600-127931600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr7:127926600-127940600	Weak transcription	Liver	Liver
34	chr7:127926600-127941400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:127926800-127940400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr7:127926800-127941400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr7:127927000-127931400	Weak transcription	Fetal Stomach	stomach
38	chr7:127927000-127932600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:127927000-127940400	Weak transcription	Aorta	Aorta
40	chr7:127927000-127940800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr7:127927000-127943200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:127927000-127944400	Weak transcription	Ovary	ovary
43	chr7:127928800-127944400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr7:127929000-127939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:127929000-127941600	Weak transcription	HSMMtube	muscle
46	chr7:127930400-127931400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:127930600-127931400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:127930800-127949200	Weak transcription	Fetal Kidney	kidney
49	chr7:127931000-127931200	Weak transcription	Brain Germinal Matrix	brain
50	chr7:127931000-127931400	ZNF genes & repeats	Fetal Lung	lung

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