EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-14169 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:35695350-35698240 
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
TGTGTGTGTA AAAGACAGAC ATGAGGTATA GAAGAGCAAT ATAGAGGTCT CCATATTATG 60
GGGGAACAGA CAGTCCCAGA GCAGGGAGGT CACTTGAACA GGGTCACAGA GGCAGGAGGC 120
CACGAACCTG GCTGGACACT GCAGGGCCAA GCAGGTAAAC ACTGTGCCTG ACTCGCACCC 180
AGACTTCGCA ACAACCCTAG AATATTCATA AGTCAGTAAT AATAGTGTTA CAGGAAAGGA 240
GTCCCGATCC AGACCCCAAG AGAGGGTTCT TGGATTCCCA CAAGAGAGAA TTCAGGGCAG 300
GTCCATAAAG TGAAAGCAAG TTTATTAGGA AAATAAAGGA ATAAAGAATG GCTACTCCAT 360
AGACAGAGCA GCCCCGAGGA CTGCTGGTTG CCCATTTTTA TGGTTATTTC TTGATGATAT 420
GCTACACAAG GGGTGGATTA TTCATTTCTC CCCTTTTTAG ACCATAGAGG GTAACTTCCC 480
GACATCGCCA TGGTATTTGT AAACTGTCAT GGCGCTGGTG GGAGTGTAGC AGTGAGGACG 540
ACCAGAGGTC ACTCTCGTGG CCATCTTGGT TTTGATGGGT ATTATCTGGC TTCTTTATTG 600
CATCCTGTTT TATCAGCAAG GTCTTTATGA CCTGCATCTT GTGTTGACCT CCTATCTCAC 660
CCTGTGACTC AGAATGCCTT AACCATCTGG GGATGCAGCC CAGTAAGTCT CAGCCTCATT 720
TTACCTGGCC CCTACTCAAG ATGGGGTTGC TCTGGTTCAA ACGCCTCTGA CAGGGTGACA 780
ACTGTGACCA CAACAGATTC ACAAACATGA CATTTTCAGA GAGAGGAAGG TATGCAGGGT 840
GGTGTGATTT GGAAGAGGCT GTGGGCGTAG AGGGATGGGT AATTCAGTTG GGGTGGTCAG 900
GGAGGGCTGC TTGGTGGAGG GGACTCTTGG CTGAGACCTG AGGGCTGTGA AGTTCTTAGA 960
GAAGGGTGTT CCAGGCAGAG GGAACAGCAA GCACAAAGGC CTGAGACGAG AGCTAGCTTG 1020
GTATGCAAGA GGAACAGAAA AGAGGAAGTG AGAGTAAGGC GGGGGAGGGA AGGGGCAGGG 1080
AATGGAGGCT GTGGAGAGGG GAGGGTTTCC AGGCAGCCCA GGACCCTCAA GGAGAGAAAC 1140
GTTGGATGTA GTCTCCCAGG TAGGGTCCAT CTGGCCCTTC CTCCTGGCTC CTGCGGAGTC 1200
CGAGTGGCTC TTTCCCTCCT TCCCTCCTCT CCCCTCCTCC TTCTCTCCCT CTCCATTTTC 1260
CCTGCAAGGT CTGCAGCCCA ACTCCAGCTC TCCCATTACT ACAGGGGCTG GTGGGTCCTT 1320
CTGAGCAAGA AGATGGGGCT CTTTGTCTAC AGTGTCTGTC TATAGTCATT CACCCACTCA 1380
TTCATTTAAT CATTCACTCA TTCATTCATT CATTTAGCCA CTCATTTGTC AAATATTGAT 1440
TTTTCTCAGG TGTTTTGCCC TCACAGGTCC TGCCGCCTAA AACACTGACT TCTTATCTCT 1500
CAAGGCTTTG CTTTCAACAC TGTCTCTTCC AAGACCTCTC CCTGACCACT CCCAACTTAC 1560
TAAACCCCTA TCACCCTGTT AGCTTTTGAA TGCTCTTCAT GGTAAAACAG GACAGGTTGA 1620
TGCTCTCCGG GGCTCTCTCT ACACACAAGA GAGAGATTAG CCTGACGGGC ATTCGTTTAC 1680
CCTTCTCATT TTCTTTGGGA ACCAGCCTCC CCTGCTCTTA GTCTATGTGA TTCGGACACA 1740
GCCAACTACA TTTCCCAGAT CCAGAAATGA ACACGCCATT CCAAGTAAAG CCAATGAGAG 1800
ACAGCTGCAG GACTTTTGCT GGAACTATTG GGAAAGTGGT GTTTCTTTTT CTGCTATGGT 1860
TACTTATCTG CTATGCTCTA AGCCTGGAAC TGCTGGAGGT CATCTTTGCT GCATGAAAAT 1920
GAAGTCAATA TTGAGGACAG CAGAGGTGAG AGGGAGAGAG GCATAATCCT GAGTGTATTG 1980
CAGGGGCACC TGGATCCAGC CATACCTGAA ATCCGAGACT TTCCATTCTA AGAACCAATA 2040
CATTCTCTTT GTACTTAAGC TAGTTTGGGT TTTAATCACT TGTGCCAGAA GGCCTGATTG 2100
ATAATAAAAC CTCAAAGATA AGCAGGCAGT CAAGCTTAGG TACTTTCCTT TTAAGAGATG 2160
CGGGCAGGTG CTTCCTTCTC TCAGAAACCA CTCCTCCTCT AGGACCTTCT ATTCTAAGAA 2220
GCCTGGGTGT TTGAGGTTCG TTCATCCTGA GGCATAAAAA CAAGATCAAA GTGCCAGGCC 2280
AGACGGAGGC AGAGTGTCTA CAGAAGCAGC CGTGCAACTA GCAGCAGGAA TTGGGAATCT 2340
GCATTATTAA TAAGCAAGCC CATTTTCCTT TACTTCTTTG TAAGCAGAGC CTTAATTTTA 2400
TTAGCCTGTT TATTAGCTCT GACCATGTGT TCAGAAAAAG TACCCTCAGC CTCTGAGTGA 2460
TCTAAGCCAG GCATAGTTCT CCTGTCTTCT TGTTGGTGAT TGGTTCTGGA AAAGGCTGGG 2520
ACACACTCCT GGCCAAGGAG AAGTCACAGC AGTGACTGAC TTGGAGGGGG AGTCTGCTGG 2580
GGGCTGGCTA GTGGAAGGCA TCTGGGGTAA AATGTTTTTG CTCTTAAAAA GTACTGTAGG 2640
AGGCCAGGCA TGTTGACTCA GGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGATGGGCAG 2700
ATCACTTGAG GTCAGGAGTT CGAGACCAGC CTGGACAACA TGATGAAACC CCATTTCTAT 2760
TTTTAAAAAT ACAAAAATTA GCTGGGCATG GTGGTGTGCA CCTGTAGTCC CAGCTACTCA 2820
GGAAGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGTTGCAGT GAGTGGACAT 2880
TGCACCACTA 2890