Variant report

Variant	nsv916220
Chromosome Location	chr7:71200006-71708048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1755)
CpG islands
(count:854)
Chromatin interactive
region (count:57)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1755 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:71274248-71274253	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:71617750-71618104	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:71455218-71455241	K562	blood:	n/a	n/a
4	ARID3A	chr7:71566408-71566651	K562	blood:	n/a	n/a
5	ATF1	chr7:71566508-71566836	K562	blood:	n/a	n/a
6	ATF1	chr7:71455137-71455357	K562	blood:	n/a	n/a
7	ATF1	chr7:71320278-71320343	K562	blood:	n/a	n/a
8	ATF1	chr7:71330176-71330443	K562	blood:	n/a	n/a
9	ATF1	chr7:71502563-71502734	K562	blood:	n/a	n/a
10	ATF1	chr7:71333804-71334105	K562	blood:	n/a	n/a
11	ATF1	chr7:71377822-71377845	K562	blood:	n/a	n/a
12	ATF1	chr7:71441751-71441900	K562	blood:	n/a	n/a
13	ATF1	chr7:71503138-71503299	K562	blood:	n/a	n/a
14	ATF3	chr7:71333858-71333988	K562	blood:	n/a	n/a
15	ATF3	chr7:71472043-71472292	K562	blood:	n/a	n/a
16	BACH1	chr7:71217175-71217290	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:71334847-71334848	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:71676169-71676646	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:71676233-71676530	K562	blood:	n/a	n/a
20	BACH1	chr7:71532876-71532877	K562	blood:	n/a	n/a
21	BATF	chr7:71635548-71635785	GM12878	blood:	n/a	n/a
22	BATF	chr7:71674059-71674398	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:71674079-71674389	GM12878	blood:	n/a	n/a
24	BCL3	chr7:71684529-71684809	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:71441760-71441968	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:71566539-71566915	K562	blood:	n/a	n/a
27	BHLHE40	chr7:71441508-71442071	K562	blood:	n/a	n/a
28	BHLHE40	chr7:71252643-71252726	K562	blood:	n/a	n/a
29	BHLHE40	chr7:71617595-71618001	HepG2	liver:	n/a	n/a
30	BHLHE40	chr7:71217114-71217428	K562	blood:	n/a	n/a
31	BHLHE40	chr7:71472048-71472269	HepG2	liver:	n/a	n/a
32	BHLHE40	chr7:71441707-71442056	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:71200991-71201315	K562	blood:	n/a	n/a
34	BHLHE40	chr7:71546282-71546344	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:71534366-71534433	K562	blood:	n/a	n/a
36	BHLHE40	chr7:71386975-71387014	K562	blood:	n/a	n/a
37	BHLHE40	chr7:71588969-71589244	HepG2	liver:	n/a	n/a
38	BHLHE40	chr7:71437671-71437780	K562	blood:	n/a	n/a
39	BHLHE40	chr7:71471980-71472347	K562	blood:	n/a	n/a
40	BHLHE40	chr7:71200790-71200796	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:71482409-71482546	K562	blood:	n/a	n/a
42	BHLHE40	chr7:71255076-71255449	K562	blood:	n/a	n/a
43	BRCA1	chr7:71217262-71217265	HepG2	liver:	n/a	n/a
44	BRCA1	chr7:71255074-71255274	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:71201122-71201244	HepG2	liver:	n/a	n/a
46	CBX3	chr7:71226341-71226613	K562	blood:	n/a	n/a
47	CBX3	chr7:71252502-71252855	K562	blood:	n/a	n/a
48	CBX3	chr7:71226361-71226624	K562	blood:	n/a	n/a
49	CBX3	chr7:71252511-71252835	K562	blood:	n/a	n/a
50	CBX3	chr7:71390710-71390864	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71217278-71217328	U87	brain:	n/a
2	chr7:71578347-71578397	PrEC	prostate:	n/a
3	chr7:71578347-71578397	AG04449	skin:	fetal
4	chr7:71407306-71407356	SKMC	muscle:	n/a
5	chr7:71217407-71217457	HMEC	breast:	n/a
6	chr7:71407390-71407440	Hela-S3	cervix:	n/a
7	chr7:71217407-71217457	AG09319	gingival:	n/a
8	chr7:71248649-71248699	ECC-1	luminal epithelium:	n/a
9	chr7:71217320-71217370	AG04450	lung:	fetal
10	chr7:71217124-71217174	PrEC	prostate:	n/a
11	chr7:71407390-71407440	HMEC	breast:	n/a
12	chr7:71682306-71682356	MCF10A-Er-Src	breast:	n/a
13	chr7:71407448-71407498	SKMC	muscle:	n/a
14	chr7:71407448-71407498	Caco-2	colon:	n/a
15	chr7:71217407-71217457	HRE	kidney:	n/a
16	chr7:71407306-71407356	MCF10A-Er-Src	breast:	n/a
17	chr7:71217407-71217457	HCM	heart:	n/a
18	chr7:71578347-71578397	Caco-2	colon:	n/a
19	chr7:71217407-71217457	HRPEpiC	eye:	n/a
20	chr7:71407306-71407356	HCM	heart:	n/a
21	chr7:71407306-71407356	HRE	kidney:	n/a
22	chr7:71217765-71217815	CMK	blood:	n/a
23	chr7:71217320-71217370	Jurkat	blood:	n/a
24	chr7:71205692-71205742	GM12891	blood:	n/a
25	chr7:71248649-71248699	HepG2	liver:	n/a
26	chr7:71202674-71202724	HUVEC	blood vessel:	n/a
27	chr7:71217278-71217328	AG09309	skin:	n/a
28	chr7:71203155-71203205	HL-60	blood:	n/a
29	chr7:71203155-71203205	NHBE	bronchial:	n/a
30	chr7:71217124-71217174	PANC-1	pancreas:	n/a
31	chr7:71217765-71217815	HUVEC	blood vessel:	n/a
32	chr7:71217765-71217815	SK-N-MC	brain:	n/a
33	chr7:71217407-71217457	SK-N-MC	brain:	n/a
34	chr7:71407306-71407356	SK-N-SH	brain:	n/a
35	chr7:71217320-71217370	U87	brain:	n/a
36	chr7:71217320-71217370	ProgFib	skin:	n/a
37	chr7:71407448-71407498	Jurkat	blood:	n/a
38	chr7:71682306-71682356	HRCEpiC	kidney:	n/a
39	chr7:71217278-71217328	Caco-2	colon:	n/a
40	chr7:71217124-71217174	T-47D	breast:	n/a
41	chr7:71205692-71205742	HCT-116	colon:	n/a
42	chr7:71578347-71578397	BE2_C	brain:	n/a
43	chr7:71217278-71217328	LNCaP	prostate:	n/a
44	chr7:71202674-71202724	Hepatocyte	liver:	n/a
45	chr7:71407448-71407498	LNCaP	prostate:	n/a
46	chr7:71203155-71203205	HUVEC	blood vessel:	n/a
47	chr7:71578347-71578397	HL-60	blood:	n/a
48	chr7:71407448-71407498	BE2_C	brain:	n/a
49	chr7:71217278-71217328	AG04450	lung:	fetal
50	chr7:71407306-71407356	GM12878	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:71248094..71249916-chr7:71251469..71253401,2	K562	blood:
2	chr7:71544603..71546705-chr7:71548451..71549976,2	K562	blood:
3	chr7:71389179..71391286-chr7:71396356..71398267,2	K562	blood:
4	chr7:71390493..71391255-chr7:71799190..71800147,2	MCF-7	breast:
5	chr20:48663617..48664420-chr7:71258548..71259048,2	Hela-S3	cervix:
6	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
7	chr1:64494077..64494875-chr7:71705794..71706323,2	MCF-7	breast:
8	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
9	chr7:71292070..71293639-chr7:71294974..71296981,2	K562	blood:
10	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
11	chr7:71333279..71335851-chr7:71388173..71390730,2	K562	blood:
12	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
13	chr7:71333255..71335073-chr7:71338385..71340355,2	K562	blood:
14	chr7:71628262..71630650-chr7:71934094..71936911,2	K562	blood:
15	chr7:71333255..71335073-chr7:71338385..71340355,2	K562	blood:
16	chr7:71334378..71336604-chr7:71338899..71340825,2	K562	blood:
17	chr7:71642905..71645487-chr7:71655969..71658022,2	K562	blood:
18	chr7:71273667..71275295-chr7:71283228..71286089,2	MCF-7	breast:
19	chr7:71389179..71391286-chr7:71396356..71398267,2	K562	blood:
20	chr7:71663421..71665320-chr7:71669615..71672136,2	K562	blood:
21	chr7:71642905..71645487-chr7:71655969..71658022,2	K562	blood:
22	chr7:71366724..71369667-chr7:71370975..71373704,2	K562	blood:
23	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
24	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:
25	chr7:71336149..71336845-chr7:71534184..71534711,2	MCF-7	breast:
26	chr7:71217131..71217801-chr7:72100027..72100693,2	MCF-7	breast:
27	chr7:71452826..71454470-chr7:71455028..71457199,2	MCF-7	breast:
28	chr7:71430764..71432829-chr7:71445344..71447656,2	K562	blood:
29	chr7:71698392..71700394-chr7:71705051..71707157,2	K562	blood:
30	chr7:71292070..71293639-chr7:71294974..71296981,2	K562	blood:
31	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
32	chr7:71648521..71649566-chr7:71958858..71959802,3	MCF-7	breast:
33	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
34	chr7:71318085..71319740-chr7:71534697..71536684,2	K562	blood:
35	chr7:71333279..71335851-chr7:71388173..71390730,2	K562	blood:
36	chr7:71336149..71336845-chr7:71534184..71534711,2	MCF-7	breast:
37	chr20:55776981..55777965-chr7:71231490..71232123,2	MCF-7	breast:
38	chr7:71526544..71528574-chr7:71533413..71536214,2	K562	blood:
39	chr7:71273667..71275295-chr7:71283228..71286089,2	MCF-7	breast:
40	chr7:71452826..71454470-chr7:71455028..71457199,2	MCF-7	breast:
41	chr7:71593896..71596339-chr7:71598361..71599867,2	K562	blood:
42	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:
43	chr7:71216886..71217682-chr7:71958728..71959690,3	K562	blood:
44	chr7:71544603..71546705-chr7:71548451..71549976,2	K562	blood:
45	chr7:71318085..71319740-chr7:71534697..71536684,2	K562	blood:
46	chr7:71390296..71390850-chr7:71798734..71799708,2	K562	blood:
47	chr7:71663421..71665320-chr7:71669615..71672136,2	K562	blood:
48	chr7:71366724..71369667-chr7:71370975..71373704,2	K562	blood:
49	chr7:71248094..71249916-chr7:71251469..71253401,2	K562	blood:
50	chr15:82275396..82277038-chr7:71501737..71504586,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALN1-2	chr7:71244476-71246986	NONHSAT121356

No data

Variant related genes	Relation type
RNA5SP232	TF binding region
ABCF2P2	TF binding region
ENSG00000235581	TF binding region
RNA5SP232	CpG island
ABCF2P2	CpG island
ENSG00000235581	CpG island
ENSG00000204580	chromatin interactions
ENSG00000207190	chromatin interactions

Extended variants
information (count: 22252 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:22252 , 50 per page) page: 1 2 3 4 5 6 7 ... 446

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190932468	chr7:71200010-71200011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73356199	chr7:71200049-71200050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117202640	chr7:71200086-71200087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs677014	chr7:71200151-71200152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs182725913	chr7:71200198-71200199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143179400	chr7:71200208-71200209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556162734	chr7:71200239-71200240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146656055	chr7:71200241-71200242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139764877	chr7:71200250-71200251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185861613	chr7:71200280-71200281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191759703	chr7:71200304-71200305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs540462002	chr7:71200321-71200322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561849579	chr7:71200374-71200375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532691126	chr7:71200387-71200388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529218765	chr7:71200408-71200409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183222543	chr7:71200409-71200410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs499526	chr7:71200411-71200412	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs532749760	chr7:71200418-71200419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562013100	chr7:71200436-71200437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188081728	chr7:71200462-71200463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566490794	chr7:71200529-71200530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs678869	chr7:71200540-71200541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs678873	chr7:71200547-71200548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs142965890	chr7:71200586-71200587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538154488	chr7:71200591-71200592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371981525	chr7:71200683-71200684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556400428	chr7:71200715-71200716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs151096800	chr7:71200759-71200760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs495858	chr7:71200790-71200791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190911168	chr7:71200804-71200805	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs10595894	chr7:71200824-71200825	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs73356201	chr7:71200848-71200849	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs376203694	chr7:71200893-71200894	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs570839653	chr7:71200899-71200900	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs141042038	chr7:71200904-71200905	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs182343620	chr7:71200928-71200929	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs573832957	chr7:71200933-71200934	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs78125576	chr7:71200964-71200965	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs150229512	chr7:71200989-71200990	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs373742166	chr7:71201022-71201023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147905844	chr7:71201024-71201025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544703173	chr7:71201111-71201112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187716299	chr7:71201138-71201139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114823754	chr7:71201164-71201165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115465845	chr7:71201203-71201204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs584390	chr7:71201212-71201213	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531828593	chr7:71201220-71201221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549960163	chr7:71201266-71201267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192525397	chr7:71201282-71201283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147042110	chr7:71201336-71201337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Autism	21865298	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1746 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71197600-71204800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:71197800-71200800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:71198000-71200800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr7:71198000-71200800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:71198000-71201200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr7:71198000-71204400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:71198400-71200800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:71198600-71200600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:71198600-71200600	Weak transcription	Fetal Muscle Leg	muscle
10	chr7:71198600-71200800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:71198600-71200800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr7:71198600-71200800	Weak transcription	Liver	Liver
13	chr7:71198800-71200800	Weak transcription	Dnd41	blood
14	chr7:71200600-71201400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:71200800-71201000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:71200800-71201000	Enhancers	Brain Substantia Nigra	brain
17	chr7:71200800-71201000	Enhancers	Fetal Muscle Leg	muscle
18	chr7:71200800-71201000	Enhancers	Rectal Smooth Muscle	rectum
19	chr7:71200800-71201000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
20	chr7:71200800-71201200	Enhancers	Liver	Liver
21	chr7:71200800-71201200	Enhancers	Brain Cingulate Gyrus	brain
22	chr7:71200800-71201200	Enhancers	Dnd41	blood
23	chr7:71200800-71201400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:71200800-71201400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:71200800-71201400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr7:71200800-71201400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr7:71200800-71201400	Enhancers	Fetal Stomach	stomach
28	chr7:71200800-71201600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:71200800-71201600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:71200800-71201600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:71201000-71201200	Enhancers	Duodenum Mucosa	Duodenum
32	chr7:71201200-71201600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:71201400-71204200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:71201400-71204400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:71201400-71204400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:71201400-71204400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr7:71201400-71204600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr7:71201600-71204400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr7:71201600-71204400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr7:71201600-71204400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr7:71204200-71205600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:71204200-71206000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:71204400-71204800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:71204400-71205000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr7:71204400-71205400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:71204400-71205400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:71204400-71205400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:71204400-71205400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr7:71204400-71205600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:71204400-71205600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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