Variant report

Variant	nsv1016231
Chromosome Location	chr5:97206242-97420435
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	ATF2	chr5:97224125-97224557	GM12878	blood:	n/a	n/a
2	ATF2	chr5:97224163-97224479	GM12878	blood:	n/a	n/a
3	BACH1	chr5:97386385-97386732	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:97224123-97224497	GM12878	blood:	n/a	n/a
5	BATF	chr5:97405650-97405889	GM12878	blood:	n/a	chr5:97405750-97405760 chr5:97405746-97405756
6	BATF	chr5:97224132-97224459	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:97224159-97224505	GM12878	blood:	n/a	chr5:97224311-97224320
8	BCL11A	chr5:97259838-97260091	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:97224140-97224399	GM12878	blood:	n/a	chr5:97224311-97224320
10	BCL11A	chr5:97378749-97378960	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr5:97224086-97224486	GM12878	blood:	n/a	chr5:97224311-97224320
12	BHLHE40	chr5:97224143-97224411	GM12878	blood:	n/a	n/a
13	CEBPB	chr5:97403339-97403649	HepG2	liver:	n/a	chr5:97403516-97403527
14	CEBPB	chr5:97288323-97288547	HepG2	liver:	n/a	chr5:97288387-97288400 chr5:97288387-97288400 chr5:97288519-97288532
15	CEBPB	chr5:97315569-97315781	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:97324361-97324490	H1-hESC	embryonic stem cell:	n/a	chr5:97324472-97324483
17	CEBPB	chr5:97394376-97394700	HepG2	liver:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
18	CEBPB	chr5:97335052-97335326	HepG2	liver:	n/a	chr5:97335304-97335315 chr5:97335304-97335313
19	CEBPB	chr5:97403339-97403632	IMR90	lung:	n/a	chr5:97403516-97403527
20	CEBPB	chr5:97256659-97256920	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:97378783-97379050	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:97398022-97398187	A549	lung:	n/a	chr5:97398105-97398116
23	CEBPB	chr5:97252023-97252330	IMR90	lung:	n/a	chr5:97252182-97252193
24	CEBPB	chr5:97252072-97252272	A549	lung:	n/a	chr5:97252182-97252193
25	CEBPB	chr5:97252040-97252324	HepG2	liver:	n/a	chr5:97252182-97252193
26	CEBPB	chr5:97227985-97228252	IMR90	lung:	n/a	chr5:97228176-97228188 chr5:97228138-97228151 chr5:97228138-97228151 chr5:97228138-97228149 chr5:97228139-97228150
27	CEBPB	chr5:97394381-97394670	A549	lung:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
28	CEBPB	chr5:97227989-97228292	HepG2	liver:	n/a	chr5:97228176-97228188 chr5:97228138-97228151 chr5:97228138-97228151 chr5:97228138-97228149 chr5:97228139-97228150
29	CEBPB	chr5:97386400-97386600	K562	blood:	n/a	chr5:97386563-97386574
30	CEBPB	chr5:97325294-97325607	IMR90	lung:	n/a	n/a
31	CEBPB	chr5:97414103-97414348	A549	lung:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
32	CEBPB	chr5:97386430-97386669	A549	lung:	n/a	chr5:97386563-97386574
33	CEBPB	chr5:97397977-97398256	HepG2	liver:	n/a	chr5:97398105-97398116
34	CEBPB	chr5:97403393-97403603	A549	lung:	n/a	chr5:97403516-97403527
35	CEBPB	chr5:97385404-97385851	HepG2	liver:	n/a	chr5:97385748-97385759 chr5:97385748-97385761 chr5:97385748-97385759
36	CEBPB	chr5:97386405-97386694	MCF-7	breast:	n/a	chr5:97386563-97386574
37	CEBPB	chr5:97386366-97386723	IMR90	lung:	n/a	chr5:97386563-97386574
38	CEBPB	chr5:97324575-97324602	A549	lung:	n/a	n/a
39	CEBPB	chr5:97414072-97414411	HepG2	liver:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
40	CEBPB	chr5:97386386-97386756	Hela-S3	cervix:	n/a	chr5:97386563-97386574
41	CEBPB	chr5:97324370-97324626	HepG2	liver:	n/a	chr5:97324472-97324483
42	CEBPB	chr5:97397978-97398244	IMR90	lung:	n/a	chr5:97398105-97398116
43	CEBPB	chr5:97386421-97386690	HepG2	liver:	n/a	chr5:97386563-97386574
44	CHD2	chr5:97386435-97386634	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr5:97259772-97260470	GM12878	blood:	n/a	n/a
46	CTCF	chr5:97353060-97353230	GM12878	blood:	n/a	n/a
47	CTCF	chr5:97366120-97366270	BJ	skin:	n/a	n/a
48	CTCF	chr5:97366120-97366270	HCT-116	colon:	n/a	n/a
49	CTCF	chr5:97389453-97389482	GM10248	blood:	n/a	n/a
50	CTCF	chr5:97321900-97322050	HCPEpiC	choroid plexus:	n/a	chr5:97322002-97322018 chr5:97321996-97322017 chr5:97322001-97322019

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97315689-97315739	HAEpiC	amniotic membrane:	n/a
2	chr5:97315689-97315739	HAEpiC	amniotic membrane:	n/a
3	chr5:97315689-97315739	HCM	heart:	n/a
4	chr5:97315689-97315739	IMR90	lung:	fetal
5	chr5:97315689-97315739	AG04449	skin:	fetal
6	chr5:97315689-97315739	SAEC	small airway:	n/a
7	chr5:97315689-97315739	T-47D	breast:	n/a
8	chr5:97315689-97315739	Hela-S3	cervix:	n/a
9	chr5:97315689-97315739	GM06990	blood:	n/a
10	chr5:97315689-97315739	HEEpiC	esophagus:	n/a
11	chr5:97315689-97315739	PrEC	prostate:	n/a
12	chr5:97315689-97315739	NHDF-neo	bronchial:	n/a
13	chr5:97315689-97315739	HEK293	kidney:	embryo
14	chr5:97315689-97315739	HCF	heart:	n/a
15	chr5:97315689-97315739	AG10803	skin:	n/a
16	chr5:97315689-97315739	HUVEC	blood vessel:	n/a
17	chr5:97315689-97315739	SK-N-MC	brain:	n/a
18	chr5:97315689-97315739	LNCaP	prostate:	n/a
19	chr5:97315689-97315739	ProgFib	skin:	n/a
20	chr5:97315689-97315739	HNPCEpiC	eye:	n/a
21	chr5:97315689-97315739	HRPEpiC	eye:	n/a
22	chr5:97315689-97315739	HIPEpiC	eye:	n/a
23	chr5:97315689-97315739	Hepatocyte	liver:	n/a
24	chr5:97315689-97315739	AG09309	skin:	n/a
25	chr5:97315689-97315739	A549	lung:	n/a
26	chr5:97315689-97315739	HMEC	breast:	n/a
27	chr5:97315689-97315739	MCF10A-Er-Src	breast:	n/a
28	chr5:97315689-97315739	HRE	kidney:	n/a
29	chr5:97315689-97315739	BJ	skin:	n/a
30	chr5:97315689-97315739	HCPEpiC	choroid plexus:	n/a
31	chr5:97315689-97315739	NH-A	brain:	n/a
32	chr5:97315689-97315739	PFSK-1	brain:	n/a
33	chr5:97315689-97315739	Jurkat	blood:	n/a
34	chr5:97315689-97315739	CMK	blood:	n/a
35	chr5:97315689-97315739	GM19239	blood:	n/a
36	chr5:97315689-97315739	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:97315689-97315739	AG04450	lung:	fetal
38	chr5:97315689-97315739	MCF-7	breast:	n/a
39	chr5:97315689-97315739	AoSMC	blood vessel:	n/a
40	chr5:97315689-97315739	U87	brain:	n/a
41	chr5:97315689-97315739	Caco-2	colon:	n/a
42	chr5:97315689-97315739	SK-N-SH	brain:	n/a
43	chr5:97315689-97315739	GM12891	blood:	n/a
44	chr5:97315689-97315739	RPTEC	kidney:	n/a
45	chr5:97315689-97315739	HepG2	liver:	n/a
46	chr5:97315689-97315739	NT2-D1	testis:	n/a
47	chr5:97315689-97315739	ovcar-3	ovarian:	n/a
48	chr5:97315689-97315739	K562	blood:	n/a
49	chr5:97315689-97315739	ECC-1	luminal epithelium:	n/a
50	chr5:97315689-97315739	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
2	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
3	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
4	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
5	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
6	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
7	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-3	chr5:97217132-97217271	XLOC_004484
2	lnc-CTD-2215E18.1.1-3	chr5:97235342-97235457	XLOC_004484
3	lnc-CTD-2215E18.1.1-3	chr5:97217124-97217271	XLOC_004484
4	lnc-CTD-2215E18.1.1-3	chr5:97257835-97258399	XLOC_004484

Variant related genes	Relation type
ENSG00000248202	TF binding region
ENSG00000249101	TF binding region
ENSG00000248202	CpG island
ENSG00000249101	CpG island
DNAJB12	miRNA target sites

Extended variants
information (count: 4674 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4674 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34550006	chr5:97209803-97209804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535133166	chr5:97209808-97209809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74798440	chr5:97209809-97209810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542153024	chr5:97209817-97209818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554036934	chr5:97209825-97209826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372834828	chr5:97209829-97209830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571311191	chr5:97209838-97209839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572600115	chr5:97209848-97209849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12515542	chr5:97209849-97209850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374079365	chr5:97209854-97209855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532253835	chr5:97209856-97209857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200122346	chr5:97209857-97209858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543947905	chr5:97209871-97209872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs180918815	chr5:97209873-97209874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529703148	chr5:97209879-97209880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548548883	chr5:97209886-97209887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544533780	chr5:97209902-97209903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527551676	chr5:97209912-97209913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561006943	chr5:97209942-97209943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184936149	chr5:97209950-97209951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144646933	chr5:97210021-97210022	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200591015	chr5:97210024-97210025	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570527685	chr5:97210055-97210056	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367968276	chr5:97210056-97210057	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542537665	chr5:97210079-97210080	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs202238206	chr5:97210080-97210081	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs5008866	chr5:97210081-97210082	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572918936	chr5:97210095-97210096	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556352782	chr5:97210130-97210131	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568371195	chr5:97210134-97210135	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535746734	chr5:97210138-97210139	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545113234	chr5:97210165-97210166	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191446718	chr5:97210234-97210235	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182776036	chr5:97210258-97210259	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72781545	chr5:97210332-97210333	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs563167239	chr5:97210370-97210371	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530061432	chr5:97210381-97210382	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544269957	chr5:97210394-97210395	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376361891	chr5:97210442-97210443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186534367	chr5:97210487-97210488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544382892	chr5:97210586-97210587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191749673	chr5:97210604-97210605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7720207	chr5:97210613-97210614	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs182974175	chr5:97210665-97210666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546608815	chr5:97210694-97210695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146934483	chr5:97210743-97210744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551907366	chr5:97210755-97210756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs137861552	chr5:97210758-97210759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4628016	chr5:97210779-97210780	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs549913125	chr5:97210834-97210835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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	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
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
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
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
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:239 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97209800-97210000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr5:97210000-97210400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:97210000-97210400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:97210000-97210600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:97210000-97210600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:97210000-97210800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr5:97210000-97210800	Enhancers	NHDF-Ad	bronchial
8	chr5:97210200-97210600	Enhancers	HSMMtube	muscle
9	chr5:97210400-97210800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:97210800-97212800	Weak transcription	NHDF-Ad	bronchial
11	chr5:97210800-97213800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:97211400-97211800	Enhancers	Gastric	stomach
13	chr5:97211600-97212400	Enhancers	Stomach Mucosa	stomach
14	chr5:97212600-97213000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:97212800-97213600	Enhancers	NHDF-Ad	bronchial
16	chr5:97213200-97214000	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr5:97213400-97213800	Enhancers	Adipose Nuclei	Adipose
18	chr5:97213600-97213800	Enhancers	Brain Substantia Nigra	brain
19	chr5:97213600-97214000	Enhancers	Brain Anterior Caudate	brain
20	chr5:97213600-97214000	Enhancers	Brain Hippocampus Middle	brain
21	chr5:97214400-97214800	Enhancers	Brain Germinal Matrix	brain
22	chr5:97215000-97215600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:97217600-97218200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr5:97224200-97224800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:97224200-97224800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:97235200-97238200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:97238200-97239000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:97238600-97239000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:97239600-97240800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:97240200-97240800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:97240800-97245200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:97241400-97243400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr5:97241600-97241800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr5:97241600-97241800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr5:97241600-97242400	Enhancers	Stomach Mucosa	stomach
36	chr5:97241600-97242600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr5:97241600-97243200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr5:97241800-97242000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr5:97241800-97242400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr5:97241800-97242400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr5:97241800-97242400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:97241800-97242400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:97241800-97242400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:97241800-97242600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr5:97242000-97242200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:97242200-97242400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr5:97242400-97242600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:97242400-97243400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:97242400-97243600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr5:97242600-97243200	Weak transcription	H1 Cell Line	embryonic stem cell

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