Variant report

Variant	nsv933161
Chromosome Location	chr5:89939500-89954066
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:89950925..89957089-chr5:90674771..90680308,6	K562	blood:
2	chr5:89703250..89710229-chr5:89936398..89944611,13	K562	blood:
3	chr5:89952329..89954940-chr5:90078278..90080126,2	K562	blood:
4	chr5:89824307..89827055-chr5:89951973..89954054,2	K562	blood:
5	chr5:89938091..89940489-chr5:89979242..89981079,3	K562	blood:
6	chr5:89953449..89955208-chr5:90677507..90679070,2	K562	blood:
7	chr5:89948021..89949895-chr5:89950501..89953146,2	MCF-7	breast:
8	chr5:89921820..89923590-chr5:89949531..89951597,2	K562	blood:
9	chr5:89702933..89707555-chr5:89951683..89956853,5	K562	blood:
10	chr5:89899642..89902183-chr5:89950994..89955309,3	K562	blood:
11	chr5:89945551..89949827-chr5:89965829..89969902,5	K562	blood:
12	chr5:89823998..89826895-chr5:89936976..89941414,5	K562	blood:
13	chr5:89706235..89707904-chr5:89940605..89942496,2	K562	blood:
14	chr5:89908957..89911258-chr5:89952267..89954603,2	K562	blood:
15	chr5:89908142..89911258-chr5:89951635..89955571,4	K562	blood:
16	chr5:89768742..89770418-chr5:89952039..89954929,2	K562	blood:
17	chr5:89899238..89902193-chr5:89950994..89956361,5	K562	blood:
18	chr5:89944237..89946798-chr5:90119584..90121436,2	K562	blood:
19	chr5:89923424..89925472-chr5:89944475..89946716,2	K562	blood:
20	chr5:89948021..89949895-chr5:89950501..89953146,2	MCF-7	breast:
21	chr5:89897975..89900696-chr5:89937499..89939734,2	K562	blood:
22	chr5:89702933..89707863-chr5:89951683..89955435,5	K562	blood:
23	chr5:89767160..89772090-chr5:89951866..89955351,7	K562	blood:
24	chr5:89768693..89770262-chr5:89940512..89942172,2	MCF-7	breast:
25	chr5:89938651..89940282-chr5:89943212..89946172,3	MCF-7	breast:
26	chr5:89950102..89952185-chr5:89967907..89971424,3	K562	blood:
27	chr5:89938077..89942103-chr5:90675427..90679817,6	K562	blood:
28	chr5:89842756..89845213-chr5:89939588..89942557,2	K562	blood:
29	chr5:89938681..89942307-chr5:90675773..90680271,6	K562	blood:
30	chr5:89703474..89706063-chr5:89939193..89940877,3	K562	blood:
31	chr5:89731732..89734444-chr5:89940233..89942146,2	K562	blood:
32	chr5:81571577..81575339-chr5:89936879..89939995,3	K562	blood:
33	chr5:89938651..89940282-chr5:89943212..89946172,3	MCF-7	breast:
34	chr5:89950917..89953812-chr5:89965739..89968417,3	K562	blood:
35	chr5:89823962..89827222-chr5:89937926..89943647,5	K562	blood:
36	chr5:89900781..89902890-chr5:89944313..89947231,2	K562	blood:
37	chr5:89951486..89954210-chr5:89956379..89958966,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000113356	chromatin interactions
ENSG00000176018	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000205464	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000164199	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000186468	chromatin interactions
ENSG00000255647	chromatin interactions

Extended variants
information (count: 587 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538502827	chr5:89939503-89939504	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs558804189	chr5:89939633-89939634	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs572283380	chr5:89939656-89939657	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs200389929	chr5:89939662-89939663	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs201007778	chr5:89939702-89939703	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs560889543	chr5:89939726-89939727	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs368383633	chr5:89939781-89939782	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs574552282	chr5:89939792-89939793	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs371906040	chr5:89939808-89939809	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs543554002	chr5:89939811-89939812	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs372642748	chr5:89939818-89939819	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs563826851	chr5:89939851-89939852	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs576814171	chr5:89939932-89939933	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs532738637	chr5:89939946-89939947	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs145616430	chr5:89939976-89939977	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs559982879	chr5:89939984-89939985	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs17620522	chr5:89940005-89940006	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs2366775	chr5:89940036-89940037	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs192845630	chr5:89940064-89940065	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs568122392	chr5:89940069-89940070	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs201586621	chr5:89940095-89940096	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs80105713	chr5:89940105-89940106	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs550656925	chr5:89940136-89940137	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs570896612	chr5:89940143-89940144	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs538810612	chr5:89940183-89940184	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs369678884	chr5:89940198-89940199	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs374271610	chr5:89940254-89940255	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs138219055	chr5:89940272-89940273	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs556084143	chr5:89940302-89940303	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs373405523	chr5:89940316-89940317	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs534932345	chr5:89940355-89940356	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs554565350	chr5:89940378-89940379	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs574489347	chr5:89940452-89940453	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs367614367	chr5:89940483-89940484	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs543492733	chr5:89940485-89940486	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs16868901	chr5:89940489-89940490	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184696502	chr5:89940504-89940505	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs78625945	chr5:89940513-89940514	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs189967386	chr5:89940528-89940529	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs267600725	chr5:89940531-89940532	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs375071987	chr5:89940541-89940542	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs369536913	chr5:89940569-89940570	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs528740341	chr5:89940579-89940580	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs372748882	chr5:89940586-89940587	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs149600158	chr5:89940588-89940589	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs199765493	chr5:89940602-89940603	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs369910075	chr5:89940608-89940609	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs373001982	chr5:89940622-89940623	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs569112173	chr5:89940636-89940637	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs397517429	chr5:89940658-89940659	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89918000-89950600	Weak transcription	Pancreas	Pancrea
2	chr5:89928800-89940000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:89928800-89941000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:89929000-89940400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:89929000-89948600	Weak transcription	Brain Anterior Caudate	brain
6	chr5:89934200-89939800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:89935800-89940000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:89935800-89941400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:89936600-89940800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr5:89936600-89940800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr5:89936600-89949000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr5:89936600-89951000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:89936800-89940800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:89936800-89941200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr5:89936800-89948600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr5:89936800-89951000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr5:89936800-89994200	Weak transcription	Brain Germinal Matrix	brain
18	chr5:89937000-89940400	Active TSS	K562	blood
19	chr5:89937000-89948600	Weak transcription	Fetal Brain Female	brain
20	chr5:89937200-89943000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:89937800-89940200	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr5:89937800-89941000	Weak transcription	HSMM	muscle
23	chr5:89938000-89940000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr5:89938200-89939600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:89938200-89940200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:89938200-89940400	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr5:89938400-89940000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:89938400-89940000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr5:89938400-89941400	Enhancers	Primary hematopoietic stem cells	blood
30	chr5:89938600-89939600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr5:89938600-89939800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:89938600-89941400	ZNF genes & repeats	GM12878-XiMat	blood
33	chr5:89939000-89940000	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr5:89939400-89939800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr5:89939600-89941400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr5:89939600-89941600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:89939800-89941200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr5:89939800-89941400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:89939800-89943000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:89940000-89940400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:89940000-89940400	Enhancers	Fetal Heart	heart
42	chr5:89940000-89941000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:89940000-89941200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr5:89940000-89941400	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:89940000-89941400	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr5:89940000-89941600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr5:89940200-89941400	Genic enhancers	HUES64 Cell Line	embryonic stem cell
48	chr5:89940200-89942400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:89940400-89940800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:89940400-89941400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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