Variant report

Variant	nsv882372
Chromosome Location	chr5:91018052-91221647
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	chr5:91090740-91091129	HepG2	liver:	n/a	n/a
2	ATF1	chr5:91148131-91148258	K562	blood:	n/a	n/a
3	BCL11A	chr5:91171038-91171201	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr5:91041790-91042000	GM12878	blood:	n/a	n/a
5	BRCA1	chr5:91093475-91093720	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr5:91144174-91144682	HCT-116	colon:	n/a	n/a
7	CBX3	chr5:91144125-91144870	HCT-116	colon:	n/a	n/a
8	CCNT2	chr5:91075961-91076161	K562	blood:	n/a	n/a
9	CCNT2	chr5:91038600-91038743	K562	blood:	n/a	n/a
10	CEBPB	chr5:91054898-91055241	A549	lung:	n/a	n/a
11	CEBPB	chr5:91077938-91078264	H1-hESC	embryonic stem cell:	n/a	chr5:91078087-91078098 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078097
12	CEBPB	chr5:91067023-91067073	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:91144102-91144750	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:91145762-91146149	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:91119557-91119748	HepG2	liver:	n/a	chr5:91119640-91119651 chr5:91119642-91119651 chr5:91119642-91119653
16	CEBPB	chr5:91181195-91181277	A549	lung:	n/a	n/a
17	CEBPB	chr5:91097703-91097916	HepG2	liver:	n/a	chr5:91097854-91097865
18	CEBPB	chr5:91209578-91209801	HepG2	liver:	n/a	chr5:91209684-91209695
19	CEBPB	chr5:91193926-91194211	HepG2	liver:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
20	CEBPB	chr5:91143989-91144785	HCT-116	colon:	n/a	n/a
21	CEBPB	chr5:91085704-91085904	A549	lung:	n/a	chr5:91085760-91085777 chr5:91085763-91085774 chr5:91085763-91085776 chr5:91085763-91085776
22	CEBPB	chr5:91221103-91221469	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:91048989-91049256	HepG2	liver:	n/a	chr5:91049145-91049156
24	CEBPB	chr5:91144308-91144641	MCF-7	breast:	n/a	n/a
25	CEBPB	chr5:91049043-91049281	A549	lung:	n/a	chr5:91049145-91049156
26	CEBPB	chr5:91048977-91049324	IMR90	lung:	n/a	chr5:91049145-91049156
27	CEBPB	chr5:91085707-91085868	IMR90	lung:	n/a	chr5:91085760-91085777 chr5:91085763-91085774 chr5:91085763-91085776 chr5:91085763-91085776
28	CEBPB	chr5:91093081-91093758	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:91077944-91078257	IMR90	lung:	n/a	chr5:91078087-91078098 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078097
30	CEBPB	chr5:91144100-91144745	HCT-116	colon:	n/a	n/a
31	CEBPB	chr5:91193946-91194198	IMR90	lung:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
32	CEBPB	chr5:91194000-91194193	H1-hESC	embryonic stem cell:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
33	CEBPB	chr5:91119513-91119708	K562	blood:	n/a	chr5:91119640-91119651 chr5:91119642-91119651 chr5:91119642-91119653
34	CEBPB	chr5:91077995-91078202	K562	blood:	n/a	chr5:91078087-91078098 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078097
35	CEBPB	chr5:91199500-91199796	H1-hESC	embryonic stem cell:	n/a	chr5:91199715-91199726
36	CEBPB	chr5:91144301-91144592	A549	lung:	n/a	n/a
37	CEBPB	chr5:91144205-91144635	A549	lung:	n/a	n/a
38	CEBPB	chr5:91144241-91144690	A549	lung:	n/a	n/a
39	CEBPB	chr5:91144946-91145322	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:91193969-91194233	A549	lung:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
41	CEBPB	chr5:91077944-91078279	HepG2	liver:	n/a	chr5:91078087-91078098 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078097
42	CEBPB	chr5:91152497-91152724	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:91152417-91152693	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr5:91144247-91144583	IMR90	lung:	n/a	n/a
45	CEBPB	chr5:91085641-91085904	HepG2	liver:	n/a	chr5:91085760-91085777 chr5:91085763-91085774 chr5:91085763-91085776 chr5:91085763-91085776
46	CEBPB	chr5:91077985-91078269	A549	lung:	n/a	chr5:91078087-91078098 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078099 chr5:91078088-91078097 chr5:91078088-91078097 chr5:91078086-91078097
47	CEBPB	chr5:91127369-91127575	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr5:91090336-91091099	A549	lung:	n/a	chr5:91090519-91090536
49	CEBPB	chr5:91083589-91083950	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:91144266-91144568	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:91137099-91137149	MCF-7	breast:	n/a
2	chr5:91018691-91018741	HRE	kidney:	n/a
3	chr5:91137099-91137149	MCF-7	breast:	n/a
4	chr5:91018691-91018741	HRE	kidney:	n/a
5	chr5:91213435-91213485	AG09309	skin:	n/a
6	chr5:91065434-91065484	HepG2	liver:	n/a
7	chr5:91065434-91065484	H1-hESC	embryonic stem cell:	embryo
8	chr5:91018691-91018741	NB4	blood:	n/a
9	chr5:91024961-91025011	HNPCEpiC	eye:	n/a
10	chr5:91018691-91018741	ProgFib	skin:	n/a
11	chr5:91065434-91065484	HMEC	breast:	n/a
12	chr5:91213435-91213485	T-47D	breast:	n/a
13	chr5:91213435-91213485	Jurkat	blood:	n/a
14	chr5:91024961-91025011	SAEC	small airway:	n/a
15	chr5:91024961-91025011	HCT-116	colon:	n/a
16	chr5:91213435-91213485	NHDF-neo	bronchial:	n/a
17	chr5:91213435-91213485	K562	blood:	n/a
18	chr5:91065434-91065484	Jurkat	blood:	n/a
19	chr5:91018691-91018741	HEEpiC	esophagus:	n/a
20	chr5:91018691-91018741	HCPEpiC	choroid plexus:	n/a
21	chr5:91018691-91018741	AG04449	skin:	fetal
22	chr5:91018691-91018741	HIPEpiC	eye:	n/a
23	chr5:91137099-91137149	HCPEpiC	choroid plexus:	n/a
24	chr5:91213435-91213485	SKMC	muscle:	n/a
25	chr5:91213190-91213240	Jurkat	blood:	n/a
26	chr5:91213190-91213240	A549	lung:	n/a
27	chr5:91137099-91137149	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:91065434-91065484	HNPCEpiC	eye:	n/a
29	chr5:91213435-91213485	U87	brain:	n/a
30	chr5:91213190-91213240	HRCEpiC	kidney:	n/a
31	chr5:91213435-91213485	Caco-2	colon:	n/a
32	chr5:91137099-91137149	NB4	blood:	n/a
33	chr5:91137099-91137149	GM19239	blood:	n/a
34	chr5:91137099-91137149	SK-N-SH	brain:	n/a
35	chr5:91065434-91065484	HCT-116	colon:	n/a
36	chr5:91213435-91213485	SK-N-MC	brain:	n/a
37	chr5:91024961-91025011	BJ	skin:	n/a
38	chr5:91213435-91213485	A549	lung:	n/a
39	chr5:91018691-91018741	HAEpiC	amniotic membrane:	n/a
40	chr5:91213435-91213485	AG04450	lung:	fetal
41	chr5:91024961-91025011	SK-N-MC	brain:	n/a
42	chr5:91213190-91213240	T-47D	breast:	n/a
43	chr5:91213435-91213485	GM12878	blood:	n/a
44	chr5:91018691-91018741	GM06990	blood:	n/a
45	chr5:91018691-91018741	MCF-7	breast:	n/a
46	chr5:91213190-91213240	PFSK-1	brain:	n/a
47	chr5:91137099-91137149	LNCaP	prostate:	n/a
48	chr5:91213190-91213240	Hela-S3	cervix:	n/a
49	chr5:91213190-91213240	AG09319	gingival:	n/a
50	chr5:91137099-91137149	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:91148456..91150162-chr5:91156168..91158769,2	K562	blood:
2	chr5:91039027..91041123-chr5:91048755..91051046,2	MCF-7	breast:
3	chr5:91165736..91168298-chr5:91169196..91172814,3	K562	blood:
4	chr5:91194593..91196093-chr6:26282424..26284564,2	MCF-7	breast:
5	chr5:91056474..91059248-chr5:91069526..91072280,3	MCF-7	breast:
6	chr5:91039027..91041123-chr5:91048755..91051046,2	MCF-7	breast:
7	chr5:91148456..91150162-chr5:91156168..91158769,2	K562	blood:
8	chr5:91164822..91166961-chr5:91195203..91197338,2	K562	blood:
9	chr5:91056474..91059248-chr5:91069526..91072280,3	MCF-7	breast:
10	chr5:91100711..91102288-chr5:91114486..91116676,2	MCF-7	breast:
11	chr5:91100711..91102288-chr5:91114486..91116676,2	MCF-7	breast:
12	chr5:91165736..91168298-chr5:91169196..91172814,3	K562	blood:
13	chr5:91164818..91166462-chr5:91169540..91172351,2	MCF-7	breast:
14	chr5:91164818..91166462-chr5:91169540..91172351,2	MCF-7	breast:
15	chr5:91164129..91166638-chr5:91167068..91169772,2	MCF-7	breast:
16	chr5:91164822..91166961-chr5:91195203..91197338,2	K562	blood:
17	chr5:91164129..91166638-chr5:91167068..91169772,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARRDC3-10	chr5:91139504-91140346	NONHSAT102766

Variant related genes	Relation type
PCBP2P3	TF binding region
PCBP2P3	CpG island

Extended variants
information (count: 5191 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5191 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2202510	chr5:91018052-91018053	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556555903	chr5:91018111-91018112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369227561	chr5:91018128-91018129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575440179	chr5:91018159-91018160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190931847	chr5:91018194-91018195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529372678	chr5:91018365-91018366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199760068	chr5:91018373-91018374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182597216	chr5:91018380-91018381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138947066	chr5:91018404-91018405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539908794	chr5:91018416-91018417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372596493	chr5:91018427-91018428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559839432	chr5:91018511-91018512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35013513	chr5:91018528-91018529	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs74733464	chr5:91018554-91018555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562548285	chr5:91018570-91018571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531861671	chr5:91018602-91018603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188901848	chr5:91018692-91018693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545691720	chr5:91018718-91018719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565300506	chr5:91018729-91018730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527908515	chr5:91018737-91018738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548038599	chr5:91018805-91018806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142865652	chr5:91018852-91018853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs193143509	chr5:91018895-91018896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374047736	chr5:91018900-91018901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549905304	chr5:91018921-91018922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535026360	chr5:91018973-91018974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369866973	chr5:91018974-91018975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35254675	chr5:91018976-91018977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570037613	chr5:91018986-91018987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537710394	chr5:91019043-91019044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558049505	chr5:91019086-91019087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4106575	chr5:91019126-91019127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115346782	chr5:91019195-91019196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533708004	chr5:91019210-91019211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551659810	chr5:91019238-91019239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559014040	chr5:91019244-91019245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79533734	chr5:91019251-91019252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573358129	chr5:91019295-91019296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542756626	chr5:91019349-91019350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555878223	chr5:91019366-91019367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576023393	chr5:91019403-91019404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557302069	chr5:91019405-91019406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545356480	chr5:91019458-91019459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147425595	chr5:91019484-91019485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183034495	chr5:91019506-91019507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35776142	chr5:91019536-91019537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541598025	chr5:91019561-91019562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111500231	chr5:91019625-91019626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530214464	chr5:91019626-91019627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74812135	chr5:91019671-91019672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91014200-91026000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:91017000-91019400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr5:91017000-91023600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:91017000-91024200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:91017400-91020600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:91017600-91018800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:91017800-91018200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr5:91018200-91018600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:91018200-91021600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr5:91018600-91018800	Enhancers	H1 Cell Line	embryonic stem cell
11	chr5:91018600-91019200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:91018800-91022000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:91018800-91022800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr5:91019200-91022000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr5:91019400-91021800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr5:91019800-91020000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:91020000-91022000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:91020600-91022000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr5:91020600-91022200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr5:91021600-91022400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:91021800-91024600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:91022000-91022200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:91022000-91024200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:91022000-91024400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:91022000-91024600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:91022200-91022800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:91022200-91023200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:91022400-91023400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr5:91022400-91023400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr5:91022600-91023200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:91022800-91023000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr5:91022800-91023200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:91023000-91023400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr5:91023200-91023400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr5:91023200-91023400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:91023200-91024000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr5:91023400-91023600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:91023400-91023600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:91023400-91024000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr5:91023400-91024400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr5:91023400-91024600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:91023600-91023800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr5:91023600-91024400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr5:91023800-91024800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:91024000-91024400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr5:91024000-91024400	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr5:91024200-91024400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr5:91024400-91025800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr5:91024600-91025600	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr5:91024600-91036800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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