EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-07613 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr19:35695310-35698140 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:35696563-35696581CCCTCCTTCCCTCCTCTC-6.33
EWSR1-FLI1MA0149.1chr19:35696559-35696577CTTTCCCTCCTTCCCTCC-7.22
GATA2MA0036.3chr19:35696839-35696850TTCTTATCTCT+6.32
Gata1MA0035.3chr19:35696839-35696850TTCTTATCTCT+6.32
Gata4MA0482.1chr19:35696840-35696851TCTTATCTCTC+6.32
MEF2CMA0497.1chr19:35698104-35698119TTCTATTTTTAAAAA-6.3
Myod1MA0499.1chr19:35697146-35697159AGAGACAGCTGCA-6.36
MyogMA0500.1chr19:35697149-35697160GACAGCTGCAG+6.62
ONECUT1MA0679.1chr19:35696781-35696795AATATTGATTTTTC-6.76
ONECUT2MA0756.1chr19:35696781-35696795AATATTGATTTTTC-6.75
ONECUT3MA0757.1chr19:35696781-35696795AATATTGATTTTTC-6.92
POU4F2MA0683.1chr19:35697688-35697704CTGCATTATTAATAAG+6.4
SPI1MA0080.4chr19:35696386-35696400GAAAAGAGGAAGTG+6.92
Tcf12MA0521.1chr19:35697149-35697160GACAGCTGCAG+6.14
ZNF263MA0528.1chr19:35696575-35696596CCTCTCCCCTCCTCCTTCTCT-6.54
ZNF263MA0528.1chr19:35696559-35696580CTTTCCCTCCTTCCCTCCTCT-6.88
ZNF263MA0528.1chr19:35696569-35696590TTCCCTCCTCTCCCCTCCTCC-7.65
ZNF263MA0528.1chr19:35696572-35696593CCTCCTCTCCCCTCCTCCTTC-8.15
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_10316chr19:35694706-35699540CD19_Primary
SE_11602chr19:35693742-35708404CD20
SE_11952chr19:35694362-35699527CD3
SE_14788chr19:35693951-35699612CD4_Memory_Primary_7pool
SE_15612chr19:35695871-35699271CD4_Memory_Primary_8pool
SE_15961chr19:35695886-35699340CD4_Naive_Primary_7pool
SE_16561chr19:35696013-35697479CD4_Naive_Primary_8pool
SE_16561chr19:35697481-35698658CD4_Naive_Primary_8pool
SE_20324chr19:35694235-35695603CD56
SE_20324chr19:35695762-35706055CD56
SE_21443chr19:35695519-35699393CD8_Memory_7pool
SE_21632chr19:35696466-35699556CD8_Naive_7pool
SE_22136chr19:35695876-35699598CD8_Naive_8pool
SE_22903chr19:35695804-35699515CD8_primiary
SE_43856chr19:35694166-35699480MM1S
SE_62877chr19:35694122-35708296Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr193569637335696472
chr193569710735697194
Number: 1             
IDChromosomeStartEnd
GH19I035202chr193569341435699474
Enhancer Sequence
ACCTGCACCA CAGCCATGCA CACACACGTG TGTGTGTGTG TGTGTGTGTA AAAGACAGAC 60
ATGAGGTATA GAAGAGCAAT ATAGAGGTCT CCATATTATG GGGGAACAGA CAGTCCCAGA 120
GCAGGGAGGT CACTTGAACA GGGTCACAGA GGCAGGAGGC CACGAACCTG GCTGGACACT 180
GCAGGGCCAA GCAGGTAAAC ACTGTGCCTG ACTCGCACCC AGACTTCGCA ACAACCCTAG 240
AATATTCATA AGTCAGTAAT AATAGTGTTA CAGGAAAGGA GTCCCGATCC AGACCCCAAG 300
AGAGGGTTCT TGGATTCCCA CAAGAGAGAA TTCAGGGCAG GTCCATAAAG TGAAAGCAAG 360
TTTATTAGGA AAATAAAGGA ATAAAGAATG GCTACTCCAT AGACAGAGCA GCCCCGAGGA 420
CTGCTGGTTG CCCATTTTTA TGGTTATTTC TTGATGATAT GCTACACAAG GGGTGGATTA 480
TTCATTTCTC CCCTTTTTAG ACCATAGAGG GTAACTTCCC GACATCGCCA TGGTATTTGT 540
AAACTGTCAT GGCGCTGGTG GGAGTGTAGC AGTGAGGACG ACCAGAGGTC ACTCTCGTGG 600
CCATCTTGGT TTTGATGGGT ATTATCTGGC TTCTTTATTG CATCCTGTTT TATCAGCAAG 660
GTCTTTATGA CCTGCATCTT GTGTTGACCT CCTATCTCAC CCTGTGACTC AGAATGCCTT 720
AACCATCTGG GGATGCAGCC CAGTAAGTCT CAGCCTCATT TTACCTGGCC CCTACTCAAG 780
ATGGGGTTGC TCTGGTTCAA ACGCCTCTGA CAGGGTGACA ACTGTGACCA CAACAGATTC 840
ACAAACATGA CATTTTCAGA GAGAGGAAGG TATGCAGGGT GGTGTGATTT GGAAGAGGCT 900
GTGGGCGTAG AGGGATGGGT AATTCAGTTG GGGTGGTCAG GGAGGGCTGC TTGGTGGAGG 960
GGACTCTTGG CTGAGACCTG AGGGCTGTGA AGTTCTTAGA GAAGGGTGTT CCAGGCAGAG 1020
GGAACAGCAA GCACAAAGGC CTGAGACGAG AGCTAGCTTG GTATGCAAGA GGAACAGAAA 1080
AGAGGAAGTG AGAGTAAGGC GGGGGAGGGA AGGGGCAGGG AATGGAGGCT GTGGAGAGGG 1140
GAGGGTTTCC AGGCAGCCCA GGACCCTCAA GGAGAGAAAC GTTGGATGTA GTCTCCCAGG 1200
TAGGGTCCAT CTGGCCCTTC CTCCTGGCTC CTGCGGAGTC CGAGTGGCTC TTTCCCTCCT 1260
TCCCTCCTCT CCCCTCCTCC TTCTCTCCCT CTCCATTTTC CCTGCAAGGT CTGCAGCCCA 1320
ACTCCAGCTC TCCCATTACT ACAGGGGCTG GTGGGTCCTT CTGAGCAAGA AGATGGGGCT 1380
CTTTGTCTAC AGTGTCTGTC TATAGTCATT CACCCACTCA TTCATTTAAT CATTCACTCA 1440
TTCATTCATT CATTTAGCCA CTCATTTGTC AAATATTGAT TTTTCTCAGG TGTTTTGCCC 1500
TCACAGGTCC TGCCGCCTAA AACACTGACT TCTTATCTCT CAAGGCTTTG CTTTCAACAC 1560
TGTCTCTTCC AAGACCTCTC CCTGACCACT CCCAACTTAC TAAACCCCTA TCACCCTGTT 1620
AGCTTTTGAA TGCTCTTCAT GGTAAAACAG GACAGGTTGA TGCTCTCCGG GGCTCTCTCT 1680
ACACACAAGA GAGAGATTAG CCTGACGGGC ATTCGTTTAC CCTTCTCATT TTCTTTGGGA 1740
ACCAGCCTCC CCTGCTCTTA GTCTATGTGA TTCGGACACA GCCAACTACA TTTCCCAGAT 1800
CCAGAAATGA ACACGCCATT CCAAGTAAAG CCAATGAGAG ACAGCTGCAG GACTTTTGCT 1860
GGAACTATTG GGAAAGTGGT GTTTCTTTTT CTGCTATGGT TACTTATCTG CTATGCTCTA 1920
AGCCTGGAAC TGCTGGAGGT CATCTTTGCT GCATGAAAAT GAAGTCAATA TTGAGGACAG 1980
CAGAGGTGAG AGGGAGAGAG GCATAATCCT GAGTGTATTG CAGGGGCACC TGGATCCAGC 2040
CATACCTGAA ATCCGAGACT TTCCATTCTA AGAACCAATA CATTCTCTTT GTACTTAAGC 2100
TAGTTTGGGT TTTAATCACT TGTGCCAGAA GGCCTGATTG ATAATAAAAC CTCAAAGATA 2160
AGCAGGCAGT CAAGCTTAGG TACTTTCCTT TTAAGAGATG CGGGCAGGTG CTTCCTTCTC 2220
TCAGAAACCA CTCCTCCTCT AGGACCTTCT ATTCTAAGAA GCCTGGGTGT TTGAGGTTCG 2280
TTCATCCTGA GGCATAAAAA CAAGATCAAA GTGCCAGGCC AGACGGAGGC AGAGTGTCTA 2340
CAGAAGCAGC CGTGCAACTA GCAGCAGGAA TTGGGAATCT GCATTATTAA TAAGCAAGCC 2400
CATTTTCCTT TACTTCTTTG TAAGCAGAGC CTTAATTTTA TTAGCCTGTT TATTAGCTCT 2460
GACCATGTGT TCAGAAAAAG TACCCTCAGC CTCTGAGTGA TCTAAGCCAG GCATAGTTCT 2520
CCTGTCTTCT TGTTGGTGAT TGGTTCTGGA AAAGGCTGGG ACACACTCCT GGCCAAGGAG 2580
AAGTCACAGC AGTGACTGAC TTGGAGGGGG AGTCTGCTGG GGGCTGGCTA GTGGAAGGCA 2640
TCTGGGGTAA AATGTTTTTG CTCTTAAAAA GTACTGTAGG AGGCCAGGCA TGTTGACTCA 2700
GGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGATGGGCAG ATCACTTGAG GTCAGGAGTT 2760
CGAGACCAGC CTGGACAACA TGATGAAACC CCATTTCTAT TTTTAAAAAT ACAAAAATTA 2820
GCTGGGCATG 2830