EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-48839 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr9:134148380-134151240 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZfxMA0146.2chr9:134150300-134150314CCCGCCGGGGCCTG+6.63
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_09361chr9:134139000-134155281CD14
SE_10759chr9:134143273-134152169CD19_Primary
SE_11405chr9:134127138-134155283CD20
SE_12146chr9:134140786-134152032CD3
SE_13249chr9:134146535-134152005CD34_Primary_RO01480
SE_13579chr9:134145384-134153422CD34_Primary_RO01536
SE_14464chr9:134140589-134153386CD4_Memory_Primary_7pool
SE_15482chr9:134143082-134154522CD4_Memory_Primary_8pool
SE_15960chr9:134147499-134153365CD4_Naive_Primary_7pool
SE_16450chr9:134143278-134153332CD4_Naive_Primary_8pool
SE_17086chr9:134145471-134153371CD4p_CD225int_CD127p_Tmem
SE_17445chr9:134129893-134155392CD4p_CD25-_CD45RAp_Naive
SE_17921chr9:134138953-134155283CD4p_CD25-_CD45ROp_Memory
SE_18747chr9:134138719-134152312CD4p_CD25-_Il17-_PMAstim_Th
SE_19407chr9:134140914-134153408CD4p_CD25-_Il17p_PMAstim_Th17
SE_20268chr9:134140912-134152219CD56
SE_20819chr9:134140943-134154649CD8_Memory_7pool
SE_21594chr9:134148326-134153391CD8_Naive_7pool
SE_22019chr9:134138986-134154667CD8_Naive_8pool
SE_22737chr9:134140797-134152275CD8_primiary
SE_25701chr9:134148325-134153466DND41
SE_29891chr9:134144371-134152234Fetal_Muscle
SE_31045chr9:134148281-134152271Fetal_Thymus
SE_39941chr9:134148334-134155326K562
SE_40648chr9:134140790-134155979Left_Ventricle
SE_42331chr9:134143355-134155429Lung
SE_43702chr9:134147115-134153210MM1S
SE_48088chr9:134142990-134160738Psoas_Muscle
SE_48582chr9:134148331-134156218Right_Atrium
SE_49606chr9:134148358-134153423Right_Ventricle
SE_50385chr9:134143341-134154692Sigmoid_Colon
SE_51267chr9:134143282-134155398Skeletal_Muscle
SE_52980chr9:134143382-134153401Small_Intestine
SE_53628chr9:134143390-134154370Spleen
SE_55150chr9:134148383-134153547Thymus
SE_59220chr9:134127420-134154306Ly3
SE_61761chr9:134100900-134154925Toledo
SE_62280chr9:134108336-134154785Tonsil
SE_67312chr9:134147115-134153210MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr9134148506134148775
chr9134149357134149638
chr9134150177134150420
Enhancer Sequence
GCTTCTATTT CCATTCAGCA AGGAGCTAAA GCAAGGCCGC ATCCTGGCCT TCTCCATGAG 60
CCCTTCAAGG GTGCAGGTTG AATCCGGGAC TCTGTTCTTT GGTAACTCGG CCCCTTAGGA 120
TGATTCTGTT GATTACTACC AAGTACTCGG CAGCCTCCTC CTCTACGTCT CAGCCACAGG 180
ACGGTCACCC ATACTGGCCT CTCGCTGAAT CCTCACAGCA GCCTACGGGA AGTTCTCCCC 240
CTCATGGACG GACACCAAAC GGAACCCCGG GGGCTGCCTG GCCAAGGCCT AGGAGCCAAG 300
ACACGTGGAC CCTTCTGCCC GACTGCTCCA AGCCGCCCCT CCCAGGAAGC TTCTGACTCC 360
ATCCTGTCCC TGGGGCTGGT CCCCGTGTAT CCCAACCGGG ATTGCACAGC CAGTGCACCC 420
AGGGAGAATG AGCTGGGTGG GACACAGAGG CTCCCTGCAG CAAAAGAGGA GTCCCGAGAG 480
CGAGAGGGAG CAAAGAGAAA CATCAGGGGC AGAGAGAGAA CAAGGAAAAT GGCCTGGAGC 540
CACTTTAAAA CGCAAGTTCT TCATGCCTTA CACTGCTTTA AAAAGTTTTA AACTCAGGAA 600
GTGGGCCCTA CGTGACAGAG AAAGACTCGG CCTGGGGAGA AAATTCACTA CACGGTGTGG 660
CTGACATCTG TCCTAATTCT GTAGTTTTAG CCACTCACAT CTGATAGAAT AACAGTAACA 720
ATCACAACAC CGCTAAGGAT GATCCCCATC CCATTACTGC CTGCGGTAAG TATTCACCAC 780
CAGCTTGGCG CAGGGCTGAC TGCATGGCGA ATTTGGTTAG CTTGAGTGAT TCTCACAATA 840
AGCCATGGGG AAGGGGTTCT TGCCAGCCCC AGTTTGCAGA TGTGTAAACT GAGGGTCAGA 900
GCAGTAAAGG GACTTGCCTA GGGCCACATC CTGGAGAGTG GCAGAACCTG GCCTCCCGCC 960
CAGATCTGCC TAAGAAGGCA TGAGGCTCTT CCAACCAGGA AGCCAGGACT GCGACAGGGA 1020
GGGCAGGGTT GTCTCAGGTC CCAGTCTCAG GCCTAGCTCC AGCCACATCA CCCACACCTA 1080
CTCAGGGTCA CCAGATGGAG AACAAGTCTT AGACAAGACA TCGGAAGCCC ATGTGCACAG 1140
ATGGGGAAGC TGAGGCTTGG AGTCTGTACC TTGGGTCAGG CCTGTGGCCT CCCCACCACA 1200
CGTTGCACCA ACCACATTAG CATCCAGTCC CGTGAGTGCT CATGTCTTTC CAAGTTCAGA 1260
AGAACCCACT GGCTTCCTTA CCCCTTCCAG GGAAGAAACT AGGCTTAGCC CAAAACCCCG 1320
AGGAAAACTT TTGTTTCTAC AACTGTCCCG ATGCCTTCAA AGCCCGAGGA GGTTTCTGGG 1380
CTTAAGCGTT CTTAGAAAAG GTCCTCACTG CATAACTAAG AATCATGTTT CCCTGCTTAG 1440
AACAGAAAGG CAGCACCCCC TCCCCCGAAC TGGATTACTA GCTGCTCTTG AGACACAAAG 1500
GGGTTGGCAC AGAAATCAGG CTGGTGGAGA GGGCCGGTGA GAGCCTCTAG ATGTGCCCCC 1560
CATGTACCTC TTTGGGACAG TCACTGTCAC ACGCTGGACT TAAGGGTTAC TGTGATCCTC 1620
ATGTTTCCTT TAGAACTTTG GAGTCATTAA GTAGAGAAGC CACCAGACTT GGTGTCCCGC 1680
CATCCTCCAC CCCTCTCATT TACAGGTGGC CCATGAGATT CTTAAATCTG TGATAAGTTC 1740
CAGCTCCTGG GGAAATTCTC CTCTTTTCCC CACTTGCAAA ACGGGGACGT GAAGCTGCAC 1800
AGGGTAGACA CTGAGAGAGG CTCTGGGAGT GTCAGCGGCC AGTCACGGGG CCACAGGGTA 1860
GACACTGAGA GAGGTTCTGG GAGTGTCAGC GGCCAGTCAC GGGGCCGCAT GGGTGGGCTG 1920
CCCGCCGGGG CCTGCCTAGC TCTCTCCAAA GGGTCCTTAC GCTCAGAAAC AGCTATTTTC 1980
ACCATCCCTG TCTTAGGGTG AACCTTCAGA TTAAGTCACT CTCCCAACTC TGCCTAAATG 2040
CAGCTCTTTT CACCCTGGGG ACGGCCTTCT CTGGGGTCAG GAAGCAGGCC AGGAAAGGAG 2100
CCCCAGGGTC CCAGGGTCCT CACCGGGACC CCCAATACCC TAGGCACACT CTGGAGACCG 2160
GGCTTTGGGG CTGCAGAGGA GAGGCTCCTC TTTGCTGTTC CTGTTAGGGC CTCGCCAGAG 2220
GGACACTGGA CTTGTCTGCA TAAAGCGGTC TTCTGCCTTG GAGACAGAAA GCGATACACT 2280
GTGAAGAAAT CGGGCTTCTA AAACTAACTG TGCTCTCAAA CACAGTGCCG TTTGGAACGG 2340
GGAAGCACTC CCCCAGCTCC TGGCATACAC TGGTAAAAGC CAGAAAGATA ATTGAGGCCC 2400
AATCGCAAAG CCCTGAACAC ACCGGTCTGG GAGTTGCAGA GTGCCTGAAT GTCTGCCATG 2460
GGCCCGCACA GGGCCAGAGG CCTGGAGGGC AGCCCTGCAG CCTCTCTGGT GACCCCTGAT 2520
GGCACAGACA CTCCTCAGGC GGACGGCACA CTTGCTCTGC CAGGAAACAC TGGGAGTAAT 2580
GTCTCTCTGC TTTCTCGGCA TCTTGCAGGG AAGGACACAG GAACCCGGGG GGAACAGTGG 2640
CAGGGTAGAT TGCAGGACCG TGACTCCAAT CTGGATCCAC AGGCAAACTT TTCAGGGAGC 2700
CACCGGGCCA ATGAGGCCAC CTGCATACCT GCCTAAAGCT TCCCTCTGGC CTCCGTCCTG 2760
TCTTCATGGT ATCTCCACCT TCCCCCTATC CGCGGCCCCC CACCAGGCCT CCAAGCTCGG 2820
CCATCCCTAG CAGTTCCCAG AGCTGGCTCT CGGCCGTACT 2860