Variant report

Variant	nsv831023
Chromosome Location	chr7:71443549-71588033
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	ARID3A	chr7:71455218-71455241	K562	blood:	n/a	n/a
2	ARID3A	chr7:71566408-71566651	K562	blood:	n/a	n/a
3	ATF1	chr7:71455137-71455357	K562	blood:	n/a	n/a
4	ATF1	chr7:71503138-71503299	K562	blood:	n/a	n/a
5	ATF1	chr7:71502563-71502734	K562	blood:	n/a	n/a
6	ATF1	chr7:71566508-71566836	K562	blood:	n/a	n/a
7	ATF3	chr7:71472043-71472292	K562	blood:	n/a	n/a
8	BACH1	chr7:71532876-71532877	K562	blood:	n/a	n/a
9	BHLHE40	chr7:71472048-71472269	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:71534366-71534433	K562	blood:	n/a	n/a
11	BHLHE40	chr7:71482409-71482546	K562	blood:	n/a	n/a
12	BHLHE40	chr7:71471980-71472347	K562	blood:	n/a	n/a
13	BHLHE40	chr7:71546282-71546344	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:71566539-71566915	K562	blood:	n/a	n/a
15	CCNT2	chr7:71566482-71566783	K562	blood:	n/a	n/a
16	CEBPB	chr7:71452403-71452765	IMR90	lung:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
17	CEBPB	chr7:71538123-71538417	K562	blood:	n/a	n/a
18	CEBPB	chr7:71518448-71518660	A549	lung:	n/a	chr7:71518594-71518607
19	CEBPB	chr7:71487571-71487779	HepG2	liver:	n/a	chr7:71487689-71487700 chr7:71487688-71487701 chr7:71487688-71487699
20	CEBPB	chr7:71452385-71452754	MCF-7	breast:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
21	CEBPB	chr7:71518411-71518720	HepG2	liver:	n/a	chr7:71518594-71518607
22	CEBPB	chr7:71520530-71520682	HepG2	liver:	n/a	chr7:71520613-71520624 chr7:71520612-71520623
23	CEBPB	chr7:71452405-71452773	A549	lung:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
24	CEBPB	chr7:71530782-71531127	K562	blood:	n/a	chr7:71530941-71530952
25	CEBPB	chr7:71530835-71531112	Hela-S3	cervix:	n/a	chr7:71530941-71530952
26	CEBPB	chr7:71518527-71518622	H1-hESC	embryonic stem cell:	n/a	chr7:71518594-71518607
27	CEBPB	chr7:71452436-71452755	Hela-S3	cervix:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
28	CEBPB	chr7:71452413-71452755	H1-hESC	embryonic stem cell:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
29	CEBPB	chr7:71490685-71490943	HepG2	liver:	n/a	chr7:71490814-71490827 chr7:71490814-71490825
30	CEBPB	chr7:71518428-71518648	K562	blood:	n/a	chr7:71518594-71518607
31	CEBPB	chr7:71530817-71531119	A549	lung:	n/a	chr7:71530941-71530952
32	CEBPB	chr7:71486191-71486385	HepG2	liver:	n/a	chr7:71486210-71486221
33	CEBPB	chr7:71530798-71531110	IMR90	lung:	n/a	chr7:71530941-71530952
34	CEBPB	chr7:71530781-71531134	HepG2	liver:	n/a	chr7:71530941-71530952
35	CEBPB	chr7:71452326-71452772	HepG2	liver:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
36	CEBPB	chr7:71452347-71452765	K562	blood:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
37	CEBPB	chr7:71530790-71531096	H1-hESC	embryonic stem cell:	n/a	chr7:71530941-71530952
38	CEBPD	chr7:71566329-71566957	K562	blood:	n/a	n/a
39	CEBPD	chr7:71566388-71566939	K562	blood:	n/a	n/a
40	CTCF	chr7:71534400-71534550	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr7:71534346-71534513	HepG2	liver:	n/a	n/a
42	CTCF	chr7:71512801-71512864	Lung_OC	lung:	n/a	n/a
43	CTCF	chr7:71534408-71534509	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:71525920-71526070	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:71512730-71512794	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:71534162-71534700	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:71474589-71474646	GM13976	blood:	n/a	n/a
48	CTCF	chr7:71534384-71534504	HepG2	liver:	n/a	n/a
49	CTCF	chr7:71534440-71534590	HEK293	kidney:	n/a	n/a
50	CTCF	chr7:71524960-71525110	GM12868	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71578347-71578397	NH-A	brain:	n/a
2	chr7:71578347-71578397	HEEpiC	esophagus:	n/a
3	chr7:71578347-71578397	Hela-S3	cervix:	n/a
4	chr7:71578347-71578397	GM12891	blood:	n/a
5	chr7:71578347-71578397	AG09309	skin:	n/a
6	chr7:71578347-71578397	RPTEC	kidney:	n/a
7	chr7:71578347-71578397	NHDF-neo	bronchial:	n/a
8	chr7:71578347-71578397	IMR90	lung:	fetal
9	chr7:71578347-71578397	MCF-7	breast:	n/a
10	chr7:71578347-71578397	HUVEC	blood vessel:	n/a
11	chr7:71578347-71578397	HepG2	liver:	n/a
12	chr7:71578347-71578397	T-47D	breast:	n/a
13	chr7:71578347-71578397	NB4	blood:	n/a
14	chr7:71578347-71578397	ProgFib	skin:	n/a
15	chr7:71578347-71578397	CMK	blood:	n/a
16	chr7:71578347-71578397	SK-N-SH	brain:	n/a
17	chr7:71578347-71578397	AG04449	skin:	fetal
18	chr7:71578347-71578397	AG04450	lung:	fetal
19	chr7:71578347-71578397	ECC-1	luminal epithelium:	n/a
20	chr7:71578347-71578397	AoSMC	blood vessel:	n/a
21	chr7:71578347-71578397	MCF10A-Er-Src	breast:	n/a
22	chr7:71578347-71578397	Jurkat	blood:	n/a
23	chr7:71578347-71578397	LNCaP	prostate:	n/a
24	chr7:71578347-71578397	HCM	heart:	n/a
25	chr7:71578347-71578397	SKMC	muscle:	n/a
26	chr7:71578347-71578397	U87	brain:	n/a
27	chr7:71578347-71578397	SK-N-MC	brain:	n/a
28	chr7:71578347-71578397	Hepatocyte	liver:	n/a
29	chr7:71578347-71578397	HCT-116	colon:	n/a
30	chr7:71578347-71578397	GM12892	blood:	n/a
31	chr7:71578347-71578397	AG10803	skin:	n/a
32	chr7:71578347-71578397	BJ	skin:	n/a
33	chr7:71578347-71578397	HCF	heart:	n/a
34	chr7:71578347-71578397	HL-60	blood:	n/a
35	chr7:71578347-71578397	HRCEpiC	kidney:	n/a
36	chr7:71578347-71578397	A549	lung:	n/a
37	chr7:71578347-71578397	HEK293	kidney:	embryo
38	chr7:71578347-71578397	HAEpiC	amniotic membrane:	n/a
39	chr7:71578347-71578397	GM06990	blood:	n/a
40	chr7:71578347-71578397	SK-N-SH_RA	brain:	n/a
41	chr7:71578347-71578397	HMEC	breast:	n/a
42	chr7:71578347-71578397	AG09319	gingival:	n/a
43	chr7:71578347-71578397	PrEC	prostate:	n/a
44	chr7:71578347-71578397	NT2-D1	testis:	n/a
45	chr7:71578347-71578397	GM12878	blood:	n/a
46	chr7:71578347-71578397	HNPCEpiC	eye:	n/a
47	chr7:71578347-71578397	PFSK-1	brain:	n/a
48	chr7:71578347-71578397	NHBE	bronchial:	n/a
49	chr7:71578347-71578397	SAEC	small airway:	n/a
50	chr7:71578347-71578397	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:71430764..71432829-chr7:71445344..71447656,2	K562	blood:
2	chr7:71452826..71454470-chr7:71455028..71457199,2	MCF-7	breast:
3	chr15:82275396..82277038-chr7:71501737..71504586,2	MCF-7	breast:
4	chr7:71452826..71454470-chr7:71455028..71457199,2	MCF-7	breast:
5	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
6	chr6:30851925..30854155-chr7:71462779..71465346,2	MCF-7	breast:
7	chr7:71526544..71528574-chr7:71533413..71536214,2	K562	blood:
8	chr7:71336149..71336845-chr7:71534184..71534711,2	MCF-7	breast:
9	chr7:71544603..71546705-chr7:71548451..71549976,2	K562	blood:
10	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
11	chr7:71544603..71546705-chr7:71548451..71549976,2	K562	blood:
12	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
13	chr7:71526544..71528574-chr7:71533413..71536214,2	K562	blood:
14	chr7:71318085..71319740-chr7:71534697..71536684,2	K562	blood:
15	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:

Variant related genes	Relation type
ABCF2P2	TF binding region
ABCF2P2	CpG island
ENSG00000204580	chromatin interactions

Extended variants
information (count: 6242 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6242 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114960363	chr7:71443551-71443552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371517526	chr7:71443552-71443553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538073377	chr7:71443562-71443563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192544747	chr7:71443601-71443602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571559407	chr7:71443610-71443611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540937518	chr7:71443618-71443619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368982318	chr7:71443629-71443630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116626133	chr7:71443663-71443664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554064562	chr7:71443691-71443692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs917209	chr7:71443802-71443803	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs184914060	chr7:71443827-71443828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73366248	chr7:71443828-71443829	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs576032856	chr7:71443829-71443830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544039627	chr7:71443887-71443888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558872828	chr7:71443888-71443889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577325466	chr7:71443889-71443890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541327532	chr7:71443908-71443909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189749050	chr7:71443925-71443926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530050591	chr7:71443959-71443960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151090877	chr7:71443985-71443986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563853376	chr7:71444057-71444058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180870426	chr7:71444061-71444062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115396954	chr7:71444062-71444063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141023705	chr7:71444067-71444068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573305255	chr7:71444085-71444086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114127864	chr7:71444106-71444107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547731672	chr7:71444182-71444183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150224092	chr7:71444184-71444185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536278767	chr7:71444191-71444192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557653553	chr7:71444212-71444213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34598697	chr7:71444224-71444225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79222637	chr7:71444240-71444241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183885664	chr7:71444257-71444258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569769711	chr7:71444309-71444310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575258544	chr7:71444315-71444316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189402454	chr7:71444320-71444321	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181969280	chr7:71444321-71444322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185977974	chr7:71444330-71444331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541191357	chr7:71444355-71444356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553284809	chr7:71444359-71444360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574789339	chr7:71444372-71444373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145747624	chr7:71444374-71444375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536969391	chr7:71444428-71444429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190644270	chr7:71444452-71444453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546005080	chr7:71444453-71444454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62462778	chr7:71444492-71444493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532385069	chr7:71444498-71444499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547595072	chr7:71444540-71444541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566023931	chr7:71444546-71444547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77891554	chr7:71444550-71444551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71431600-71445800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:71432000-71446400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:71440400-71445400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:71441400-71452800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:71442400-71445800	Weak transcription	Thymus	Thymus
6	chr7:71443400-71445600	Strong transcription	Fetal Thymus	thymus
7	chr7:71445400-71445800	Weak transcription	Dnd41	blood
8	chr7:71445400-71447600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:71445600-71447200	Genic enhancers	Fetal Thymus	thymus
10	chr7:71445800-71447200	Genic enhancers	Thymus	Thymus
11	chr7:71445800-71448400	Enhancers	Dnd41	blood
12	chr7:71445800-71448600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:71446400-71447200	Enhancers	Primary hematopoietic stem cells	blood
14	chr7:71446800-71447400	Enhancers	Primary T cells from cord blood	blood
15	chr7:71447000-71448000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr7:71447200-71448400	Enhancers	Fetal Thymus	thymus
17	chr7:71447200-71449800	Weak transcription	Thymus	Thymus
18	chr7:71447200-71452400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr7:71447400-71447800	Weak transcription	Primary T cells from cord blood	blood
20	chr7:71447600-71448000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:71447800-71448600	Enhancers	Primary T cells from cord blood	blood
22	chr7:71448000-71448600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:71448000-71452000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr7:71448400-71449200	Weak transcription	Fetal Thymus	thymus
25	chr7:71448400-71452400	Weak transcription	Dnd41	blood
26	chr7:71448600-71451200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:71448600-71451200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr7:71448600-71453000	Weak transcription	Primary T cells from cord blood	blood
29	chr7:71449200-71450400	Genic enhancers	Fetal Thymus	thymus
30	chr7:71449800-71450400	Genic enhancers	Thymus	Thymus
31	chr7:71450400-71451000	Weak transcription	Fetal Thymus	thymus
32	chr7:71450400-71451000	Weak transcription	Thymus	Thymus
33	chr7:71451000-71454400	Enhancers	Fetal Thymus	thymus
34	chr7:71451000-71454400	Enhancers	Thymus	Thymus
35	chr7:71451200-71452800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:71451200-71453200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr7:71451400-71453800	Weak transcription	Pancreas	Pancrea
38	chr7:71452000-71452600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr7:71452000-71454000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr7:71452200-71454000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:71452400-71453000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr7:71452400-71453200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:71452400-71453400	Enhancers	Dnd41	blood
44	chr7:71452400-71454000	Enhancers	Primary hematopoietic stem cells	blood
45	chr7:71452800-71453200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:71452800-71454000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:71453000-71453400	Enhancers	Primary T cells from cord blood	blood
48	chr7:71453200-71454000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:71453200-71454000	Enhancers	Adipose Nuclei	Adipose
50	chr7:71453200-71454000	Enhancers	Brain Hippocampus Middle	brain

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