Variant report

Variant	nsv887838
Chromosome Location	chr7:20862302-21016683
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	chr7:20998893-20999302	HepG2	liver:	n/a	n/a
2	ATF1	chr7:20877207-20877333	K562	blood:	n/a	n/a
3	ATF1	chr7:20956124-20956469	K562	blood:	n/a	n/a
4	BACH1	chr7:21010431-21010433	K562	blood:	n/a	n/a
5	BACH1	chr7:20874837-20875044	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:20868703-20868705	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:20865259-20865505	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:20874996-20875153	K562	blood:	n/a	n/a
9	CBX3	chr7:20874712-20875142	K562	blood:	n/a	n/a
10	CEBPB	chr7:21003588-21004262	Hela-S3	cervix:	n/a	chr7:21004087-21004100 chr7:21003732-21003743 chr7:21004087-21004100
11	CEBPB	chr7:21003592-21003857	MCF-7	breast:	n/a	chr7:21003732-21003743
12	CEBPB	chr7:20982645-20982902	HepG2	liver:	n/a	chr7:20982787-20982798
13	CEBPB	chr7:21003695-21004267	HCT-116	colon:	n/a	chr7:21004087-21004100 chr7:21003732-21003743 chr7:21004087-21004100
14	CEBPB	chr7:20992675-20992875	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr7:21003650-21004164	K562	blood:	n/a	chr7:21004087-21004100 chr7:21003732-21003743 chr7:21004087-21004100
16	CEBPB	chr7:21003896-21004023	K562	blood:	n/a	n/a
17	CEBPB	chr7:20992727-20992809	K562	blood:	n/a	n/a
18	CEBPB	chr7:20945142-20945342	HepG2	liver:	n/a	chr7:20945231-20945242 chr7:20945230-20945243 chr7:20945230-20945243
19	CEBPB	chr7:21003744-21004216	H1-hESC	embryonic stem cell:	n/a	chr7:21004087-21004100 chr7:21004087-21004100
20	CEBPB	chr7:21003893-21004187	ECC-1	luminal epithelium:	n/a	chr7:21004087-21004100 chr7:21004087-21004100
21	CEBPB	chr7:21003638-21004295	HCT-116	colon:	n/a	chr7:21004087-21004100 chr7:21003732-21003743 chr7:21004087-21004100
22	CEBPB	chr7:20936707-20936927	A549	lung:	n/a	chr7:20936776-20936787 chr7:20936828-20936841
23	CEBPB	chr7:20945124-20945380	IMR90	lung:	n/a	chr7:20945231-20945242 chr7:20945230-20945243 chr7:20945230-20945243
24	CEBPB	chr7:20998929-20999308	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:20936715-20936972	HepG2	liver:	n/a	chr7:20936776-20936787 chr7:20936828-20936841
26	CEBPB	chr7:20898713-20899009	HepG2	liver:	n/a	chr7:20898847-20898858 chr7:20898847-20898860
27	CEBPB	chr7:20891552-20891682	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:21003596-21004230	A549	lung:	n/a	chr7:21004087-21004100 chr7:21003732-21003743 chr7:21004087-21004100
29	CEBPB	chr7:21003580-21004242	HepG2	liver:	n/a	chr7:21004087-21004100 chr7:21003732-21003743 chr7:21004087-21004100
30	CHD2	chr7:20874815-20875156	K562	blood:	n/a	n/a
31	CTCF	chr7:20874400-20874550	GM12875	blood:	n/a	chr7:20874466-20874487
32	CTCF	chr7:20874442-20874525	GM13977	blood:	n/a	chr7:20874466-20874487
33	CTCF	chr7:20874478-20874539	GM10248	blood:	n/a	n/a
34	CTCF	chr7:20953593-20953775	A549	lung:	n/a	n/a
35	CTCF	chr7:20874435-20874532	GM10266	blood:	n/a	chr7:20874466-20874487
36	CTCF	chr7:20874380-20874530	Caco-2	colon:	n/a	chr7:20874466-20874487
37	CTCF	chr7:20889155-20889305	NHEK	skin:	n/a	n/a
38	CTCF	chr7:20874440-20874590	NHEK	skin:	n/a	chr7:20874466-20874487
39	CTCF	chr7:20874420-20874570	HEEpiC	esophagus:	n/a	chr7:20874466-20874487
40	CTCF	chr7:20932575-20932622	GM10248	blood:	n/a	n/a
41	CTCF	chr7:20953620-20953770	A549	lung:	n/a	n/a
42	CTCF	chr7:20953420-20953570	A549	lung:	n/a	n/a
43	CTCF	chr7:20874420-20874570	HMEC	breast:	n/a	chr7:20874466-20874487
44	CTCF	chr7:20912449-20912462	GM10248	blood:	n/a	n/a
45	CTCF	chr7:20874399-20874546	Medullo	brain:	n/a	chr7:20874466-20874487
46	CTCF	chr7:20874460-20874610	GM12872	blood:	n/a	chr7:20874466-20874487
47	CTCF	chr7:20874387-20874582	HUVEC	blood vessel:	n/a	chr7:20874466-20874487
48	CTCF	chr7:20874740-20874890	GM06990	blood:	n/a	n/a
49	CTCF	chr7:20874440-20874590	HUVEC	blood vessel:	n/a	chr7:20874466-20874487
50	CTCF	chr7:20874400-20874550	A549	lung:	n/a	chr7:20874466-20874487

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:20992918-20992968	AG04450	lung:	fetal
2	chr7:20867067-20867117	GM19239	blood:	n/a
3	chr7:20905085-20905135	MCF10A-Er-Src	breast:	n/a
4	chr7:20865522-20865572	MCF10A-Er-Src	breast:	n/a
5	chr7:20865522-20865572	HepG2	liver:	n/a
6	chr7:20867067-20867117	GM06990	blood:	n/a
7	chr7:20865639-20865689	HRE	kidney:	n/a
8	chr7:20905085-20905135	HNPCEpiC	eye:	n/a
9	chr7:20905085-20905135	HCT-116	colon:	n/a
10	chr7:20992918-20992968	GM12891	blood:	n/a
11	chr7:20867067-20867117	AG04450	lung:	fetal
12	chr7:20867067-20867117	LNCaP	prostate:	n/a
13	chr7:20905085-20905135	PFSK-1	brain:	n/a
14	chr7:20865522-20865572	LNCaP	prostate:	n/a
15	chr7:20992918-20992968	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:20905085-20905135	HIPEpiC	eye:	n/a
17	chr7:21004288-21004338	NHDF-neo	bronchial:	n/a
18	chr7:20865522-20865572	ovcar-3	ovarian:	n/a
19	chr7:20865522-20865572	H1-hESC	embryonic stem cell:	embryo
20	chr7:20865639-20865689	BE2_C	brain:	n/a
21	chr7:20905085-20905135	NT2-D1	testis:	n/a
22	chr7:20992918-20992968	AoSMC	blood vessel:	n/a
23	chr7:20865522-20865572	NHBE	bronchial:	n/a
24	chr7:21004288-21004338	HCPEpiC	choroid plexus:	n/a
25	chr7:20865639-20865689	AG09309	skin:	n/a
26	chr7:20867067-20867117	H1-hESC	embryonic stem cell:	embryo
27	chr7:20867067-20867117	GM12891	blood:	n/a
28	chr7:20865639-20865689	HRPEpiC	eye:	n/a
29	chr7:21004288-21004338	HNPCEpiC	eye:	n/a
30	chr7:20992918-20992968	HepG2	liver:	n/a
31	chr7:20865522-20865572	GM19239	blood:	n/a
32	chr7:20905085-20905135	Hela-S3	cervix:	n/a
33	chr7:20905085-20905135	NH-A	brain:	n/a
34	chr7:20867067-20867117	SK-N-SH	brain:	n/a
35	chr7:20867067-20867117	GM12878	blood:	n/a
36	chr7:20905085-20905135	AG09309	skin:	n/a
37	chr7:20992918-20992968	SK-N-SH_RA	brain:	n/a
38	chr7:20865522-20865572	AG09319	gingival:	n/a
39	chr7:20867067-20867117	SK-N-SH_RA	brain:	n/a
40	chr7:20865639-20865689	NHDF-neo	bronchial:	n/a
41	chr7:20865639-20865689	AG04449	skin:	fetal
42	chr7:20992918-20992968	BE2_C	brain:	n/a
43	chr7:20865639-20865689	GM12878	blood:	n/a
44	chr7:20865639-20865689	A549	lung:	n/a
45	chr7:20865639-20865689	GM19239	blood:	n/a
46	chr7:20865639-20865689	H1-hESC	embryonic stem cell:	embryo
47	chr7:20905085-20905135	AG04449	skin:	fetal
48	chr7:20865639-20865689	SK-N-SH	brain:	n/a
49	chr7:21004288-21004338	MCF-7	breast:	n/a
50	chr7:20905085-20905135	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:20878635..20880252-chr7:20887810..20889362,2	MCF-7	breast:
2	chr7:20817740..20818290-chr7:20874326..20874941,2	K562	blood:
3	chr7:20906769..20909401-chr7:20920366..20921886,2	MCF-7	breast:
4	chr7:20869345..20871616-chr7:20871826..20873790,2	K562	blood:
5	chr7:20817500..20818001-chr7:20874011..20874545,2	MCF-7	breast:
6	chr7:21000665..21003909-chr7:21007145..21010992,3	K562	blood:
7	chr7:20869345..20871616-chr7:20871826..20873790,2	K562	blood:
8	chr7:20915061..20916783-chr7:20921069..20922598,2	K562	blood:
9	chr7:20976279..20978886-chr7:20978918..20980911,2	K562	blood:
10	chr7:20878635..20880252-chr7:20887810..20889362,2	MCF-7	breast:
11	chr7:20976279..20978886-chr7:20978918..20980911,2	K562	blood:
12	chr7:21000665..21003909-chr7:21007145..21010992,3	K562	blood:
13	chr7:20915061..20916783-chr7:20921069..20922598,2	K562	blood:
14	chr7:20906769..20909401-chr7:20920366..20921886,2	MCF-7	breast:
15	chr7:20835982..20838746-chr7:20913081..20916681,3	K562	blood:
16	chr7:20824901..20827825-chr7:20873586..20876476,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCB5-1	chr7:20922359-20922435	ENSG00000232790.2
2	lnc-ABCB5-1	chr7:20875050-20875123	ENSG00000232790.1
3	lnc-ABCB5-5	chr7:20970290-20970788	ucExp_206_+
4	lnc-ABCB5-3	chr7:20866998-20867169	NONHSAT119435
5	lnc-SP8-3	chr7:20970290-20970788	ucExp_206_-
6	lnc-ABCB5-3	chr7:20867861-20868017	NONHSAT119435
7	lnc-ABCB5-3	chr7:20866917-20867439	NONHSAT119434
8	lnc-ABCB5-4	chr7:20883246-20883580	NONHSAT119438
9	lnc-ABCB5-1	chr7:20875050-20875123	ENSG00000232790.2
10	lnc-ABCB5-1	chr7:20922359-20922435	ENSG00000232790.1

Variant related genes	Relation type
LINC01162	TF binding region
RPS26P30	TF binding region
RPL23P8	TF binding region
LINC01162	CpG island
RPS26P30	CpG island
RPL23P8	CpG island
ENSG00000164651	chromatin interactions

Extended variants
information (count: 3605 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3605 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565896499	chr7:20864414-20864415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535059785	chr7:20864417-20864418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531852204	chr7:20864429-20864430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373167620	chr7:20864432-20864433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376339003	chr7:20864435-20864436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369895842	chr7:20864441-20864442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541933747	chr7:20864453-20864454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111481905	chr7:20864470-20864471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373991998	chr7:20864490-20864491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538750684	chr7:20864514-20864515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192025670	chr7:20864525-20864526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202076943	chr7:20864555-20864556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56314002	chr7:20864569-20864570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538452614	chr7:20864570-20864571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550166104	chr7:20864571-20864572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562121340	chr7:20864582-20864583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571747539	chr7:20864596-20864597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141039579	chr7:20864631-20864632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555665930	chr7:20864655-20864656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184266694	chr7:20864665-20864666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544543574	chr7:20864696-20864697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144800370	chr7:20864729-20864730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138643749	chr7:20864731-20864732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377490459	chr7:20864810-20864811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545491664	chr7:20864841-20864842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560559476	chr7:20864877-20864878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539171006	chr7:20864902-20864903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527735014	chr7:20864918-20864919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375003898	chr7:20864923-20864924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140616696	chr7:20864927-20864928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145667758	chr7:20864948-20864949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547915309	chr7:20864954-20864955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188502737	chr7:20865000-20865001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549782625	chr7:20865024-20865025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564512848	chr7:20865053-20865054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538417491	chr7:20865075-20865076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553495336	chr7:20865096-20865097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565413694	chr7:20865111-20865112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180942195	chr7:20865121-20865122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186117037	chr7:20865125-20865126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs36015295	chr7:20865189-20865190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs76732969	chr7:20865191-20865192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575604966	chr7:20865203-20865204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114059941	chr7:20865249-20865250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556539025	chr7:20865254-20865255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs578154541	chr7:20865260-20865261	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs545270262	chr7:20865268-20865269	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560596662	chr7:20865321-20865322	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76315540	chr7:20865331-20865332	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs527771877	chr7:20865347-20865348	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Lung cancer	16773561	CNVD
Schizophrenia	19546859	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:20864400-20865400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr7:20865400-20866600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr7:20865400-20867000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr7:20865400-20867000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:20865400-20867000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:20865400-20867200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:20865400-20867600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:20865600-20866400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:20865600-20866600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:20865800-20866400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:20865800-20866400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:20865800-20866800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr7:20865800-20867200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:20865800-20868000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:20866000-20866600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:20866200-20866400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr7:20866200-20867400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr7:20866400-20867000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr7:20866400-20869000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr7:20866400-20870800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:20866400-20871200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:20866600-20870800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr7:20866600-20870800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:20867000-20867200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr7:20867000-20867200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:20867000-20868600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr7:20867000-20870800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:20867200-20869400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:20867200-20870800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:20867200-20871000	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:20867400-20868600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:20867600-20870800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr7:20868000-20868400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:20868400-20869600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:20868600-20868800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:20868600-20869000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:20868600-20869800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:20868800-20869200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:20869000-20869400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:20869000-20871000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr7:20869200-20869600	Enhancers	Fetal Brain Female	brain
42	chr7:20869200-20869800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr7:20869200-20869800	Enhancers	Brain Germinal Matrix	brain
44	chr7:20869200-20869800	Enhancers	Fetal Brain Male	brain
45	chr7:20869400-20869800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:20869400-20871200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:20869600-20871000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr7:20869600-20871600	Weak transcription	Fetal Brain Female	brain
49	chr7:20869800-20870800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr7:20869800-20870800	Weak transcription	Fetal Brain Male	brain

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