Variant report

Variant	nsv531373
Chromosome Location	chr7:71487076-71765613
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:366)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:71566408-71566651	K562	blood:	n/a	n/a
2	ARID3A	chr7:71617750-71618104	HepG2	liver:	n/a	n/a
3	ATF1	chr7:71502563-71502734	K562	blood:	n/a	n/a
4	ATF1	chr7:71748535-71748603	K562	blood:	n/a	n/a
5	ATF1	chr7:71503138-71503299	K562	blood:	n/a	n/a
6	ATF1	chr7:71566508-71566836	K562	blood:	n/a	n/a
7	ATF2	chr7:71730494-71730993	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:71730568-71730921	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:71676169-71676646	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:71532876-71532877	K562	blood:	n/a	n/a
11	BACH1	chr7:71676233-71676530	K562	blood:	n/a	n/a
12	BATF	chr7:71635548-71635785	GM12878	blood:	n/a	n/a
13	BATF	chr7:71674059-71674398	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:71674079-71674389	GM12878	blood:	n/a	n/a
15	BCL3	chr7:71684529-71684809	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:71588969-71589244	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:71546282-71546344	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:71617595-71618001	HepG2	liver:	n/a	n/a
19	BHLHE40	chr7:71534366-71534433	K562	blood:	n/a	n/a
20	BHLHE40	chr7:71566539-71566915	K562	blood:	n/a	n/a
21	BHLHE40	chr7:71730295-71730461	K562	blood:	n/a	n/a
22	CCNT2	chr7:71566482-71566783	K562	blood:	n/a	n/a
23	CEBPB	chr7:71729286-71729372	HepG2	liver:	n/a	chr7:71729324-71729335
24	CEBPB	chr7:71668950-71669066	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:71614550-71614874	HepG2	liver:	n/a	chr7:71614702-71614713
26	CEBPB	chr7:71530782-71531127	K562	blood:	n/a	chr7:71530941-71530952
27	CEBPB	chr7:71723120-71723245	K562	blood:	n/a	chr7:71723174-71723185
28	CEBPB	chr7:71518428-71518648	K562	blood:	n/a	chr7:71518594-71518607
29	CEBPB	chr7:71518411-71518720	HepG2	liver:	n/a	chr7:71518594-71518607
30	CEBPB	chr7:71530798-71531110	IMR90	lung:	n/a	chr7:71530941-71530952
31	CEBPB	chr7:71490685-71490943	HepG2	liver:	n/a	chr7:71490814-71490827 chr7:71490814-71490825
32	CEBPB	chr7:71530835-71531112	Hela-S3	cervix:	n/a	chr7:71530941-71530952
33	CEBPB	chr7:71530817-71531119	A549	lung:	n/a	chr7:71530941-71530952
34	CEBPB	chr7:71605041-71605227	A549	lung:	n/a	chr7:71605206-71605217
35	CEBPB	chr7:71518448-71518660	A549	lung:	n/a	chr7:71518594-71518607
36	CEBPB	chr7:71530790-71531096	H1-hESC	embryonic stem cell:	n/a	chr7:71530941-71530952
37	CEBPB	chr7:71757503-71757552	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:71630836-71631036	HepG2	liver:	n/a	chr7:71630947-71630956 chr7:71630946-71630957 chr7:71630945-71630956
39	CEBPB	chr7:71723036-71723330	IMR90	lung:	n/a	chr7:71723174-71723185
40	CEBPB	chr7:71614594-71614788	K562	blood:	n/a	chr7:71614702-71614713
41	CEBPB	chr7:71711676-71711904	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:71723050-71723323	A549	lung:	n/a	chr7:71723174-71723185
43	CEBPB	chr7:71672394-71672528	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:71538123-71538417	K562	blood:	n/a	n/a
45	CEBPB	chr7:71752628-71752861	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:71711658-71711926	K562	blood:	n/a	n/a
47	CEBPB	chr7:71520530-71520682	HepG2	liver:	n/a	chr7:71520613-71520624 chr7:71520612-71520623
48	CEBPB	chr7:71721022-71721087	HepG2	liver:	n/a	chr7:71721064-71721077
49	CEBPB	chr7:71487571-71487779	HepG2	liver:	n/a	chr7:71487689-71487700 chr7:71487688-71487701 chr7:71487688-71487699
50	CEBPB	chr7:71605024-71605315	HepG2	liver:	n/a	chr7:71605206-71605217

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71578347-71578397	HEEpiC	esophagus:	n/a
2	chr7:71578347-71578397	ovcar-3	ovarian:	n/a
3	chr7:71747028-71747078	HL-60	blood:	n/a
4	chr7:71744787-71744837	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:71747028-71747078	AG09319	gingival:	n/a
6	chr7:71578347-71578397	CMK	blood:	n/a
7	chr7:71744787-71744837	HepG2	liver:	n/a
8	chr7:71747028-71747078	HEK293	kidney:	embryo
9	chr7:71682306-71682356	HEK293	kidney:	embryo
10	chr7:71747028-71747078	ProgFib	skin:	n/a
11	chr7:71747632-71747682	Caco-2	colon:	n/a
12	chr7:71747632-71747682	HCT-116	colon:	n/a
13	chr7:71729065-71729115	GM19239	blood:	n/a
14	chr7:71747028-71747078	Hela-S3	cervix:	n/a
15	chr7:71682306-71682356	HCT-116	colon:	n/a
16	chr7:71747632-71747682	HEEpiC	esophagus:	n/a
17	chr7:71744787-71744837	NHBE	bronchial:	n/a
18	chr7:71747028-71747078	GM06990	blood:	n/a
19	chr7:71729065-71729115	H1-hESC	embryonic stem cell:	embryo
20	chr7:71747028-71747078	HCF	heart:	n/a
21	chr7:71747632-71747682	A549	lung:	n/a
22	chr7:71729065-71729115	K562	blood:	n/a
23	chr7:71744787-71744837	PrEC	prostate:	n/a
24	chr7:71747632-71747682	SK-N-SH	brain:	n/a
25	chr7:71744787-71744837	ProgFib	skin:	n/a
26	chr7:71747632-71747682	HEK293	kidney:	embryo
27	chr7:71747632-71747682	HAEpiC	amniotic membrane:	n/a
28	chr7:71744787-71744837	H1-hESC	embryonic stem cell:	embryo
29	chr7:71578347-71578397	H1-hESC	embryonic stem cell:	embryo
30	chr7:71682306-71682356	ovcar-3	ovarian:	n/a
31	chr7:71578347-71578397	HRE	kidney:	n/a
32	chr7:71747028-71747078	PrEC	prostate:	n/a
33	chr7:71682306-71682356	HRPEpiC	eye:	n/a
34	chr7:71682306-71682356	K562	blood:	n/a
35	chr7:71682306-71682356	GM12891	blood:	n/a
36	chr7:71729065-71729115	AG09309	skin:	n/a
37	chr7:71682306-71682356	SKMC	muscle:	n/a
38	chr7:71744787-71744837	SK-N-SH_RA	brain:	n/a
39	chr7:71729065-71729115	BE2_C	brain:	n/a
40	chr7:71747028-71747078	AoSMC	blood vessel:	n/a
41	chr7:71578347-71578397	PrEC	prostate:	n/a
42	chr7:71747028-71747078	HCPEpiC	choroid plexus:	n/a
43	chr7:71747632-71747682	HCM	heart:	n/a
44	chr7:71682306-71682356	ECC-1	luminal epithelium:	n/a
45	chr7:71682306-71682356	GM06990	blood:	n/a
46	chr7:71682306-71682356	NT2-D1	testis:	n/a
47	chr7:71578347-71578397	HCM	heart:	n/a
48	chr7:71747028-71747078	T-47D	breast:	n/a
49	chr7:71747028-71747078	GM12892	blood:	n/a
50	chr7:71578347-71578397	AG04449	skin:	fetal

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:71648521..71649566-chr7:71958858..71959802,3	MCF-7	breast:
2	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
3	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
4	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
5	chr7:71336149..71336845-chr7:71534184..71534711,2	MCF-7	breast:
6	chr7:71628262..71630650-chr7:71934094..71936911,2	K562	blood:
7	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
8	chr7:71642905..71645487-chr7:71655969..71658022,2	K562	blood:
9	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
10	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
11	chr7:71752349..71754126-chr7:71756443..71759399,2	K562	blood:
12	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
13	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:
14	chr7:71765415..71767059-chr7:71769100..71770926,2	K562	blood:
15	chr7:71544603..71546705-chr7:71548451..71549976,2	K562	blood:
16	chr7:71526544..71528574-chr7:71533413..71536214,2	K562	blood:
17	chr7:71593896..71596339-chr7:71598361..71599867,2	K562	blood:
18	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:
19	chr7:71642905..71645487-chr7:71655969..71658022,2	K562	blood:
20	chr7:71698392..71700394-chr7:71705051..71707157,2	K562	blood:
21	chr7:71526544..71528574-chr7:71533413..71536214,2	K562	blood:
22	chr7:71544603..71546705-chr7:71548451..71549976,2	K562	blood:
23	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
24	chr15:82275396..82277038-chr7:71501737..71504586,2	MCF-7	breast:
25	chr1:64494077..64494875-chr7:71705794..71706323,2	MCF-7	breast:
26	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
27	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
28	chr7:71593896..71596339-chr7:71598361..71599867,2	K562	blood:
29	chr7:71663421..71665320-chr7:71669615..71672136,2	K562	blood:
30	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
31	chr7:71318085..71319740-chr7:71534697..71536684,2	K562	blood:
32	chr7:71663421..71665320-chr7:71669615..71672136,2	K562	blood:
33	chr7:71698392..71700394-chr7:71705051..71707157,2	K562	blood:
34	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:
35	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:

No data

Variant related genes	Relation type
CALN1	TF binding region
ABCF2P2	TF binding region
CALN1	CpG island
ABCF2P2	CpG island
ENSG00000207190	chromatin interactions

Extended variants
information (count: 12804 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:12804 , 50 per page) page: 1 2 3 4 5 6 7 ... 257

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149331612	chr7:71487092-71487093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556097331	chr7:71487107-71487108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571664134	chr7:71487120-71487121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539091793	chr7:71487153-71487154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557694598	chr7:71487189-71487190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371269893	chr7:71487196-71487197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559920863	chr7:71487209-71487210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540582639	chr7:71487210-71487211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144843279	chr7:71487221-71487222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549553933	chr7:71487225-71487226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528033942	chr7:71487267-71487268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370649550	chr7:71487268-71487269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544244117	chr7:71487331-71487332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148251472	chr7:71487415-71487416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532914679	chr7:71487456-71487457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141244336	chr7:71487482-71487483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567983726	chr7:71487498-71487499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549276252	chr7:71487526-71487527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560562661	chr7:71487560-71487561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185147937	chr7:71487567-71487568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569091309	chr7:71487575-71487576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549119803	chr7:71487593-71487594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567627634	chr7:71487616-71487617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531848624	chr7:71487686-71487687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187305521	chr7:71487699-71487700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17428098	chr7:71487701-71487702	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571592544	chr7:71487750-71487751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190793762	chr7:71487761-71487762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183876024	chr7:71487762-71487763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550744302	chr7:71487763-71487764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370604790	chr7:71487791-71487792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186793332	chr7:71487792-71487793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570947039	chr7:71487834-71487835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533989048	chr7:71487838-71487839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555569363	chr7:71487842-71487843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574006317	chr7:71487858-71487859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201852145	chr7:71487892-71487893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373280119	chr7:71487906-71487907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539872615	chr7:71487907-71487908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74329154	chr7:71487919-71487920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368108224	chr7:71487922-71487923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs66732939	chr7:71487929-71487930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5884871	chr7:71487936-71487937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370727830	chr7:71487937-71487938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137976373	chr7:71487942-71487943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191533144	chr7:71487969-71487970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577557803	chr7:71487971-71487972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377382522	chr7:71487974-71487975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539947016	chr7:71487982-71487983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369914375	chr7:71488046-71488047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71482400-71491400	Strong transcription	Fetal Thymus	thymus
2	chr7:71483400-71492600	Weak transcription	Fetal Brain Male	brain
3	chr7:71484600-71498400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:71485600-71489200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:71485600-71489200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:71485800-71487400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:71487000-71488200	Weak transcription	Primary hematopoietic stem cells	blood
8	chr7:71487000-71493600	Strong transcription	Thymus	Thymus
9	chr7:71487400-71493200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:71487800-71493200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:71488200-71489000	Strong transcription	Primary hematopoietic stem cells	blood
12	chr7:71489000-71495000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr7:71489200-71493200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:71489200-71493200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:71490400-71490800	Enhancers	Brain Angular Gyrus	brain
16	chr7:71490400-71490800	Enhancers	Brain Substantia Nigra	brain
17	chr7:71490400-71491000	Enhancers	Brain Hippocampus Middle	brain
18	chr7:71490600-71490800	Enhancers	Brain Anterior Caudate	brain
19	chr7:71490800-71498400	Weak transcription	Brain Anterior Caudate	brain
20	chr7:71490800-71498400	Weak transcription	Brain Substantia Nigra	brain
21	chr7:71491000-71493400	Weak transcription	Brain Hippocampus Middle	brain
22	chr7:71491400-71493200	Weak transcription	Fetal Thymus	thymus
23	chr7:71492400-71493200	Weak transcription	Pancreas	Pancrea
24	chr7:71492600-71492800	Enhancers	Fetal Brain Male	brain
25	chr7:71492800-71493200	Weak transcription	Fetal Brain Male	brain
26	chr7:71493200-71493400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:71493200-71493400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr7:71493200-71493400	Enhancers	Pancreas	Pancrea
29	chr7:71493200-71493600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:71493200-71493600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:71493200-71493800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:71493200-71494400	Enhancers	Fetal Brain Male	brain
33	chr7:71493200-71494800	ZNF genes & repeats	Fetal Thymus	thymus
34	chr7:71493400-71493600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
35	chr7:71493400-71493600	Enhancers	Brain Hippocampus Middle	brain
36	chr7:71493400-71496600	Weak transcription	Pancreas	Pancrea
37	chr7:71493400-71503600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:71493600-71494200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:71493600-71494800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:71493600-71497400	Weak transcription	Brain Hippocampus Middle	brain
41	chr7:71493600-71497600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr7:71493600-71498400	Weak transcription	Thymus	Thymus
43	chr7:71493800-71494600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:71494200-71495200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:71494400-71497800	Weak transcription	Fetal Brain Male	brain
46	chr7:71494600-71495800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:71494800-71495000	Strong transcription	Fetal Thymus	thymus
48	chr7:71494800-71495400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:71495000-71495200	Strong transcription	Primary hematopoietic stem cells	blood
50	chr7:71495000-71497600	Weak transcription	Fetal Thymus	thymus

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