EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS074-07746 
Organism
Homo sapiens 
Tissue/cell
GM19239 
Coordinate
chr19:35695320-35698190 
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: 15             
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_20324chr19:35695762-35706055CD56
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
CAGCCATGCA CACACACGTG TGTGTGTGTG TGTGTGTGTA AAAGACAGAC ATGAGGTATA 60
GAAGAGCAAT ATAGAGGTCT CCATATTATG GGGGAACAGA CAGTCCCAGA GCAGGGAGGT 120
CACTTGAACA GGGTCACAGA GGCAGGAGGC CACGAACCTG GCTGGACACT GCAGGGCCAA 180
GCAGGTAAAC ACTGTGCCTG ACTCGCACCC AGACTTCGCA ACAACCCTAG AATATTCATA 240
AGTCAGTAAT AATAGTGTTA CAGGAAAGGA GTCCCGATCC AGACCCCAAG AGAGGGTTCT 300
TGGATTCCCA CAAGAGAGAA TTCAGGGCAG GTCCATAAAG TGAAAGCAAG TTTATTAGGA 360
AAATAAAGGA ATAAAGAATG GCTACTCCAT AGACAGAGCA GCCCCGAGGA CTGCTGGTTG 420
CCCATTTTTA TGGTTATTTC TTGATGATAT GCTACACAAG GGGTGGATTA TTCATTTCTC 480
CCCTTTTTAG ACCATAGAGG GTAACTTCCC GACATCGCCA TGGTATTTGT AAACTGTCAT 540
GGCGCTGGTG GGAGTGTAGC AGTGAGGACG ACCAGAGGTC ACTCTCGTGG CCATCTTGGT 600
TTTGATGGGT ATTATCTGGC TTCTTTATTG CATCCTGTTT TATCAGCAAG GTCTTTATGA 660
CCTGCATCTT GTGTTGACCT CCTATCTCAC CCTGTGACTC AGAATGCCTT AACCATCTGG 720
GGATGCAGCC CAGTAAGTCT CAGCCTCATT TTACCTGGCC CCTACTCAAG ATGGGGTTGC 780
TCTGGTTCAA ACGCCTCTGA CAGGGTGACA ACTGTGACCA CAACAGATTC ACAAACATGA 840
CATTTTCAGA GAGAGGAAGG TATGCAGGGT GGTGTGATTT GGAAGAGGCT GTGGGCGTAG 900
AGGGATGGGT AATTCAGTTG GGGTGGTCAG GGAGGGCTGC TTGGTGGAGG GGACTCTTGG 960
CTGAGACCTG AGGGCTGTGA AGTTCTTAGA GAAGGGTGTT CCAGGCAGAG GGAACAGCAA 1020
GCACAAAGGC CTGAGACGAG AGCTAGCTTG GTATGCAAGA GGAACAGAAA AGAGGAAGTG 1080
AGAGTAAGGC GGGGGAGGGA AGGGGCAGGG AATGGAGGCT GTGGAGAGGG GAGGGTTTCC 1140
AGGCAGCCCA GGACCCTCAA GGAGAGAAAC GTTGGATGTA GTCTCCCAGG TAGGGTCCAT 1200
CTGGCCCTTC CTCCTGGCTC CTGCGGAGTC CGAGTGGCTC TTTCCCTCCT TCCCTCCTCT 1260
CCCCTCCTCC TTCTCTCCCT CTCCATTTTC CCTGCAAGGT CTGCAGCCCA ACTCCAGCTC 1320
TCCCATTACT ACAGGGGCTG GTGGGTCCTT CTGAGCAAGA AGATGGGGCT CTTTGTCTAC 1380
AGTGTCTGTC TATAGTCATT CACCCACTCA TTCATTTAAT CATTCACTCA TTCATTCATT 1440
CATTTAGCCA CTCATTTGTC AAATATTGAT TTTTCTCAGG TGTTTTGCCC TCACAGGTCC 1500
TGCCGCCTAA AACACTGACT TCTTATCTCT CAAGGCTTTG CTTTCAACAC TGTCTCTTCC 1560
AAGACCTCTC CCTGACCACT CCCAACTTAC TAAACCCCTA TCACCCTGTT AGCTTTTGAA 1620
TGCTCTTCAT GGTAAAACAG GACAGGTTGA TGCTCTCCGG GGCTCTCTCT ACACACAAGA 1680
GAGAGATTAG CCTGACGGGC ATTCGTTTAC CCTTCTCATT TTCTTTGGGA ACCAGCCTCC 1740
CCTGCTCTTA GTCTATGTGA TTCGGACACA GCCAACTACA TTTCCCAGAT CCAGAAATGA 1800
ACACGCCATT CCAAGTAAAG CCAATGAGAG ACAGCTGCAG GACTTTTGCT GGAACTATTG 1860
GGAAAGTGGT GTTTCTTTTT CTGCTATGGT TACTTATCTG CTATGCTCTA AGCCTGGAAC 1920
TGCTGGAGGT CATCTTTGCT GCATGAAAAT GAAGTCAATA TTGAGGACAG CAGAGGTGAG 1980
AGGGAGAGAG GCATAATCCT GAGTGTATTG CAGGGGCACC TGGATCCAGC CATACCTGAA 2040
ATCCGAGACT TTCCATTCTA AGAACCAATA CATTCTCTTT GTACTTAAGC TAGTTTGGGT 2100
TTTAATCACT TGTGCCAGAA GGCCTGATTG ATAATAAAAC CTCAAAGATA AGCAGGCAGT 2160
CAAGCTTAGG TACTTTCCTT TTAAGAGATG CGGGCAGGTG CTTCCTTCTC TCAGAAACCA 2220
CTCCTCCTCT AGGACCTTCT ATTCTAAGAA GCCTGGGTGT TTGAGGTTCG TTCATCCTGA 2280
GGCATAAAAA CAAGATCAAA GTGCCAGGCC AGACGGAGGC AGAGTGTCTA CAGAAGCAGC 2340
CGTGCAACTA GCAGCAGGAA TTGGGAATCT GCATTATTAA TAAGCAAGCC CATTTTCCTT 2400
TACTTCTTTG TAAGCAGAGC CTTAATTTTA TTAGCCTGTT TATTAGCTCT GACCATGTGT 2460
TCAGAAAAAG TACCCTCAGC CTCTGAGTGA TCTAAGCCAG GCATAGTTCT CCTGTCTTCT 2520
TGTTGGTGAT TGGTTCTGGA AAAGGCTGGG ACACACTCCT GGCCAAGGAG AAGTCACAGC 2580
AGTGACTGAC TTGGAGGGGG AGTCTGCTGG GGGCTGGCTA GTGGAAGGCA TCTGGGGTAA 2640
AATGTTTTTG CTCTTAAAAA GTACTGTAGG AGGCCAGGCA TGTTGACTCA GGCCTGTAAT 2700
CCCAGCACTT TGGGAGGCCA AGATGGGCAG ATCACTTGAG GTCAGGAGTT CGAGACCAGC 2760
CTGGACAACA TGATGAAACC CCATTTCTAT TTTTAAAAAT ACAAAAATTA GCTGGGCATG 2820
GTGGTGTGCA CCTGTAGTCC CAGCTACTCA GGAAGCTGAG GCAGGAGAAT 2870