Variant report

Variant	nsv538929
Chromosome Location	chr7:70010392-70190353
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2304)
CpG islands
(count:2381)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2304 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70163321-70163538	K562	blood:	n/a	n/a
2	ARID3A	chr7:70102162-70102182	K562	blood:	n/a	n/a
3	ARID3A	chr7:70036382-70036767	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:70033765-70034826	K562	blood:	n/a	n/a
5	ATF1	chr7:70034407-70035107	K562	blood:	n/a	n/a
6	ATF1	chr7:70091841-70091986	K562	blood:	n/a	n/a
7	ATF1	chr7:70033782-70034115	K562	blood:	n/a	n/a
8	ATF2	chr7:70164867-70165954	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:70164947-70166179	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:70158188-70158571	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:70159737-70160179	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:70163149-70163641	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:70133624-70133911	GM12878	blood:	n/a	n/a
14	ATF2	chr7:70161308-70161791	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:70113044-70113441	GM12878	blood:	n/a	n/a
16	ATF2	chr7:70182931-70183279	GM12878	blood:	n/a	n/a
17	ATF3	chr7:70181519-70181861	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:70060789-70060989	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:70084144-70084459	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:70054021-70054368	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:70061335-70061723	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:70145962-70146088	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:70064701-70064711	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:70171826-70171998	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr7:70047222-70047546	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr7:70128632-70129069	GM12878	blood:	n/a	n/a
27	BATF	chr7:70175130-70175457	GM12878	blood:	n/a	chr7:70175301-70175311 chr7:70175300-70175311 chr7:70175171-70175180
28	BATF	chr7:70144546-70144968	GM12878	blood:	n/a	n/a
29	BATF	chr7:70113183-70113442	GM12878	blood:	n/a	n/a
30	BATF	chr7:70144538-70144907	GM12878	blood:	n/a	n/a
31	BATF	chr7:70175177-70175456	GM12878	blood:	n/a	chr7:70175301-70175311 chr7:70175300-70175311
32	BATF	chr7:70146926-70147314	GM12878	blood:	n/a	n/a
33	BATF	chr7:70128646-70129082	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:70165146-70165623	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL11A	chr7:70128600-70129082	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:70110801-70111113	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:70128594-70129058	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:70113093-70113397	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:70165263-70165600	H1-hESC	embryonic stem cell:	n/a	n/a
40	BHLHE40	chr7:70060794-70061115	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:70128509-70129192	GM12878	blood:	n/a	chr7:70128654-70128675
42	BHLHE40	chr7:70158734-70159179	GM12878	blood:	n/a	chr7:70159147-70159163
43	BHLHE40	chr7:70146929-70147278	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:70113074-70113557	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:70133463-70133982	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:70163292-70163553	K562	blood:	n/a	n/a
47	BHLHE40	chr7:70160128-70160685	GM12878	blood:	n/a	chr7:70160375-70160391
48	BHLHE40	chr7:70163235-70163633	GM12878	blood:	n/a	n/a
49	BHLHE40	chr7:70110741-70111166	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:70079192-70079569	GM12878	blood:	n/a	n/a

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70055327-70055377	GM19239	blood:	n/a
2	chr7:70085367-70085417	ovcar-3	ovarian:	n/a
3	chr7:70055327-70055377	GM19239	blood:	n/a
4	chr7:70085367-70085417	ovcar-3	ovarian:	n/a
5	chr7:70159340-70159390	SAEC	small airway:	n/a
6	chr7:70096029-70096079	HUVEC	blood vessel:	n/a
7	chr7:70038627-70038677	HepG2	liver:	n/a
8	chr7:70060835-70060885	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:70156755-70156805	HCM	heart:	n/a
10	chr7:70061135-70061185	HCT-116	colon:	n/a
11	chr7:70160006-70160056	HEK293	kidney:	embryo
12	chr7:70157145-70157195	AG10803	skin:	n/a
13	chr7:70065373-70065423	Hela-S3	cervix:	n/a
14	chr7:70061455-70061505	K562	blood:	n/a
15	chr7:70061616-70061666	HCPEpiC	choroid plexus:	n/a
16	chr7:70159340-70159390	HIPEpiC	eye:	n/a
17	chr7:70156755-70156805	HCT-116	colon:	n/a
18	chr7:70159215-70159265	NB4	blood:	n/a
19	chr7:70175567-70175617	AG09309	skin:	n/a
20	chr7:70159330-70159380	RPTEC	kidney:	n/a
21	chr7:70160498-70160548	HEEpiC	esophagus:	n/a
22	chr7:70060153-70060203	Caco-2	colon:	n/a
23	chr7:70172515-70172565	ProgFib	skin:	n/a
24	chr7:70175567-70175617	CMK	blood:	n/a
25	chr7:70100095-70100145	HCM	heart:	n/a
26	chr7:70057640-70057690	HRE	kidney:	n/a
27	chr7:70085367-70085417	AG09319	gingival:	n/a
28	chr7:70159340-70159390	HUVEC	blood vessel:	n/a
29	chr7:70065373-70065423	SK-N-SH	brain:	n/a
30	chr7:70132171-70132221	HEEpiC	esophagus:	n/a
31	chr7:70038627-70038677	Hepatocyte	liver:	n/a
32	chr7:70100095-70100145	AG09309	skin:	n/a
33	chr7:70175567-70175617	Hepatocyte	liver:	n/a
34	chr7:70061135-70061185	AG04449	skin:	fetal
35	chr7:70165515-70165565	Caco-2	colon:	n/a
36	chr7:70061064-70061114	ECC-1	luminal epithelium:	n/a
37	chr7:70061455-70061505	LNCaP	prostate:	n/a
38	chr7:70132171-70132221	HL-60	blood:	n/a
39	chr7:70061064-70061114	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:70126616-70126666	SK-N-MC	brain:	n/a
41	chr7:70160734-70160784	SAEC	small airway:	n/a
42	chr7:70170620-70170670	HRCEpiC	kidney:	n/a
43	chr7:70160734-70160784	NB4	blood:	n/a
44	chr7:70158761-70158811	BE2_C	brain:	n/a
45	chr7:70172515-70172565	PFSK-1	brain:	n/a
46	chr7:70060153-70060203	T-47D	breast:	n/a
47	chr7:70061064-70061114	GM06990	blood:	n/a
48	chr7:70126616-70126666	GM12892	blood:	n/a
49	chr7:70038627-70038677	ProgFib	skin:	n/a
50	chr7:70038627-70038677	T-47D	breast:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70116058..70119019-chr7:70120958..70123553,2	K562	blood:
2	chr7:70069205..70071813-chr7:70077445..70079383,2	K562	blood:
3	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
4	chr7:70049785..70050737-chr7:70162923..70163511,2	MCF-7	breast:
5	chr7:70041903..70043590-chr7:70046514..70049488,2	K562	blood:
6	chr7:70157686..70159380-chr7:70159994..70162274,2	MCF-7	breast:
7	chr7:70029430..70032358-chr7:70034724..70037517,2	K562	blood:
8	chr7:70182197..70184832-chr7:70191535..70193515,2	MCF-7	breast:
9	chr7:70035377..70037187-chr7:70048714..70051712,2	MCF-7	breast:
10	chr7:70048823..70050343-chr7:70052305..70054085,2	K562	blood:
11	chr7:70174321..70176691-chr7:70186792..70188789,2	MCF-7	breast:
12	chr7:70133847..70137058-chr7:70140413..70143195,3	K562	blood:
13	chr7:70029430..70032358-chr7:70034724..70037517,2	K562	blood:
14	chr7:70184183..70185798-chr7:70197589..70200298,2	MCF-7	breast:
15	chr7:70133847..70137058-chr7:70140413..70143195,3	K562	blood:
16	chr7:70174321..70176691-chr7:70186792..70188789,2	MCF-7	breast:
17	chr7:69507259..69508393-chr7:70162935..70163782,5	MCF-7	breast:
18	chr7:70092147..70095006-chr7:70098737..70101187,2	K562	blood:
19	chr7:70084622..70086291-chr7:70088234..70089854,2	K562	blood:
20	chr7:70116058..70119019-chr7:70120958..70123553,2	K562	blood:
21	chr7:70175580..70177405-chr7:70179545..70181681,2	MCF-7	breast:
22	chr7:70175580..70177405-chr7:70179545..70181681,2	MCF-7	breast:
23	chr7:70084622..70086291-chr7:70088234..70089854,2	K562	blood:
24	chr7:70092147..70095006-chr7:70098737..70101187,2	K562	blood:
25	chr7:70048823..70050343-chr7:70052305..70054085,2	K562	blood:
26	chr7:70035377..70037187-chr7:70048714..70051712,2	MCF-7	breast:
27	chr7:70069205..70071813-chr7:70077445..70079383,2	K562	blood:
28	chr7:70041903..70043590-chr7:70046514..70049488,2	K562	blood:
29	chr7:70049785..70050737-chr7:70162923..70163511,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WBSCR17-3	chr7:70163555-70164476	NONHSAT121336
2	lnc-CALN1-4	chr7:70085301-70085806	NONHSAT121334
3	lnc-WBSCR17-3	chr7:70159859-70160031	NONHSAT121336
4	lnc-CALN1-4	chr7:70083180-70083205	NONHSAT121334

No data

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island

Extended variants
information (count: 7011 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:7011 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114205494	chr7:70010396-70010397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372309613	chr7:70010413-70010414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79622267	chr7:70010414-70010415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139347526	chr7:70010431-70010432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs886661	chr7:70010479-70010480	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs557175308	chr7:70010495-70010496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567606524	chr7:70010531-70010532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs180689699	chr7:70010563-70010564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35977255	chr7:70010570-70010571	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs578059451	chr7:70010581-70010582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555073220	chr7:70010585-70010586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573784379	chr7:70010586-70010587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143257439	chr7:70010629-70010630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147496765	chr7:70010697-70010698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs13227106	chr7:70010730-70010731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs115206122	chr7:70010734-70010735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561531917	chr7:70010764-70010765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572759894	chr7:70010794-70010795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544283912	chr7:70010828-70010829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562476255	chr7:70010829-70010830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148539028	chr7:70010868-70010869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532740842	chr7:70010890-70010891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142851764	chr7:70010926-70010927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150636804	chr7:70011026-70011027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527586520	chr7:70011058-70011059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549054988	chr7:70011086-70011087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567446382	chr7:70011097-70011098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531441793	chr7:70011103-70011104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115879952	chr7:70011110-70011111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571789978	chr7:70011141-70011142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185888264	chr7:70011169-70011170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554217802	chr7:70011184-70011185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369460943	chr7:70011193-70011194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117067001	chr7:70011212-70011213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2866715	chr7:70011308-70011309	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs188646598	chr7:70011338-70011339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576562616	chr7:70011355-70011356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543678081	chr7:70011379-70011380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575826500	chr7:70011381-70011382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577330429	chr7:70011425-70011426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs118028609	chr7:70011434-70011435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143584798	chr7:70011447-70011448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544032726	chr7:70011467-70011468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556335486	chr7:70011540-70011541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527346656	chr7:70011576-70011577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542893461	chr7:70011620-70011621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182120871	chr7:70011631-70011632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544438633	chr7:70011634-70011635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377208342	chr7:70011638-70011639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531504363	chr7:70011675-70011676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4144 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69995400-70012200	Weak transcription	Fetal Stomach	stomach
2	chr7:69996800-70017800	Weak transcription	Aorta	Aorta
3	chr7:70000200-70015400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr7:70006000-70011600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:70008600-70019600	Weak transcription	Psoas Muscle	Psoas
6	chr7:70008800-70010400	Enhancers	Fetal Brain Female	brain
7	chr7:70009400-70011000	Enhancers	Primary B cells from peripheral blood	blood
8	chr7:70009600-70010600	Weak transcription	Fetal Muscle Leg	muscle
9	chr7:70009600-70012400	Weak transcription	Fetal Brain Male	brain
10	chr7:70010000-70010800	Enhancers	GM12878-XiMat	blood
11	chr7:70010200-70012400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:70010600-70010800	Enhancers	Fetal Muscle Leg	muscle
13	chr7:70011000-70022800	Weak transcription	Primary B cells from peripheral blood	blood
14	chr7:70012200-70012400	ZNF genes & repeats	Fetal Stomach	stomach
15	chr7:70012400-70012800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:70012600-70036800	Weak transcription	Fetal Stomach	stomach
17	chr7:70012800-70014600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:70012800-70022600	Weak transcription	Primary B cells from cord blood	blood
19	chr7:70013200-70016200	Weak transcription	Fetal Brain Male	brain
20	chr7:70014600-70015200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:70015000-70015800	Weak transcription	Ovary	ovary
22	chr7:70015200-70023200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:70015800-70016000	Enhancers	Ovary	ovary
24	chr7:70016000-70033600	Weak transcription	Ovary	ovary
25	chr7:70016200-70018600	Enhancers	Fetal Brain Male	brain
26	chr7:70016800-70018200	Enhancers	Fetal Brain Female	brain
27	chr7:70016800-70018400	Enhancers	Brain Hippocampus Middle	brain
28	chr7:70017400-70017800	Enhancers	Brain Germinal Matrix	brain
29	chr7:70017400-70019800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:70017600-70018600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
31	chr7:70017800-70018600	Enhancers	Brain Anterior Caudate	brain
32	chr7:70018000-70018600	Enhancers	Brain Cingulate Gyrus	brain
33	chr7:70018000-70018800	Enhancers	Liver	Liver
34	chr7:70018200-70018400	Enhancers	Brain Substantia Nigra	brain
35	chr7:70018200-70018600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr7:70018200-70022200	Weak transcription	Fetal Brain Female	brain
37	chr7:70018400-70018600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:70018400-70018600	Enhancers	Brain Angular Gyrus	brain
39	chr7:70018400-70018600	Enhancers	Gastric	stomach
40	chr7:70018400-70019600	Weak transcription	Brain Substantia Nigra	brain
41	chr7:70018400-70026600	Weak transcription	Brain Hippocampus Middle	brain
42	chr7:70018600-70019800	Weak transcription	Brain Anterior Caudate	brain
43	chr7:70018600-70026600	Weak transcription	Brain Angular Gyrus	brain
44	chr7:70018600-70030200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr7:70018600-70030400	Weak transcription	Gastric	stomach
46	chr7:70018600-70033800	Weak transcription	Fetal Brain Male	brain
47	chr7:70018800-70021800	Weak transcription	Liver	Liver
48	chr7:70019400-70020600	Enhancers	Fetal Muscle Leg	muscle
49	chr7:70019600-70019800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:70019600-70019800	Enhancers	Psoas Muscle	Psoas

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