EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS180-24267 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr19:35695950-35698590 
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
CATCCTGTTT TATCAGCAAG GTCTTTATGA CCTGCATCTT GTGTTGACCT CCTATCTCAC 60
CCTGTGACTC AGAATGCCTT AACCATCTGG GGATGCAGCC CAGTAAGTCT CAGCCTCATT 120
TTACCTGGCC CCTACTCAAG ATGGGGTTGC TCTGGTTCAA ACGCCTCTGA CAGGGTGACA 180
ACTGTGACCA CAACAGATTC ACAAACATGA CATTTTCAGA GAGAGGAAGG TATGCAGGGT 240
GGTGTGATTT GGAAGAGGCT GTGGGCGTAG AGGGATGGGT AATTCAGTTG GGGTGGTCAG 300
GGAGGGCTGC TTGGTGGAGG GGACTCTTGG CTGAGACCTG AGGGCTGTGA AGTTCTTAGA 360
GAAGGGTGTT CCAGGCAGAG GGAACAGCAA GCACAAAGGC CTGAGACGAG AGCTAGCTTG 420
GTATGCAAGA GGAACAGAAA AGAGGAAGTG AGAGTAAGGC GGGGGAGGGA AGGGGCAGGG 480
AATGGAGGCT GTGGAGAGGG GAGGGTTTCC AGGCAGCCCA GGACCCTCAA GGAGAGAAAC 540
GTTGGATGTA GTCTCCCAGG TAGGGTCCAT CTGGCCCTTC CTCCTGGCTC CTGCGGAGTC 600
CGAGTGGCTC TTTCCCTCCT TCCCTCCTCT CCCCTCCTCC TTCTCTCCCT CTCCATTTTC 660
CCTGCAAGGT CTGCAGCCCA ACTCCAGCTC TCCCATTACT ACAGGGGCTG GTGGGTCCTT 720
CTGAGCAAGA AGATGGGGCT CTTTGTCTAC AGTGTCTGTC TATAGTCATT CACCCACTCA 780
TTCATTTAAT CATTCACTCA TTCATTCATT CATTTAGCCA CTCATTTGTC AAATATTGAT 840
TTTTCTCAGG TGTTTTGCCC TCACAGGTCC TGCCGCCTAA AACACTGACT TCTTATCTCT 900
CAAGGCTTTG CTTTCAACAC TGTCTCTTCC AAGACCTCTC CCTGACCACT CCCAACTTAC 960
TAAACCCCTA TCACCCTGTT AGCTTTTGAA TGCTCTTCAT GGTAAAACAG GACAGGTTGA 1020
TGCTCTCCGG GGCTCTCTCT ACACACAAGA GAGAGATTAG CCTGACGGGC ATTCGTTTAC 1080
CCTTCTCATT TTCTTTGGGA ACCAGCCTCC CCTGCTCTTA GTCTATGTGA TTCGGACACA 1140
GCCAACTACA TTTCCCAGAT CCAGAAATGA ACACGCCATT CCAAGTAAAG CCAATGAGAG 1200
ACAGCTGCAG GACTTTTGCT GGAACTATTG GGAAAGTGGT GTTTCTTTTT CTGCTATGGT 1260
TACTTATCTG CTATGCTCTA AGCCTGGAAC TGCTGGAGGT CATCTTTGCT GCATGAAAAT 1320
GAAGTCAATA TTGAGGACAG CAGAGGTGAG AGGGAGAGAG GCATAATCCT GAGTGTATTG 1380
CAGGGGCACC TGGATCCAGC CATACCTGAA ATCCGAGACT TTCCATTCTA AGAACCAATA 1440
CATTCTCTTT GTACTTAAGC TAGTTTGGGT TTTAATCACT TGTGCCAGAA GGCCTGATTG 1500
ATAATAAAAC CTCAAAGATA AGCAGGCAGT CAAGCTTAGG TACTTTCCTT TTAAGAGATG 1560
CGGGCAGGTG CTTCCTTCTC TCAGAAACCA CTCCTCCTCT AGGACCTTCT ATTCTAAGAA 1620
GCCTGGGTGT TTGAGGTTCG TTCATCCTGA GGCATAAAAA CAAGATCAAA GTGCCAGGCC 1680
AGACGGAGGC AGAGTGTCTA CAGAAGCAGC CGTGCAACTA GCAGCAGGAA TTGGGAATCT 1740
GCATTATTAA TAAGCAAGCC CATTTTCCTT TACTTCTTTG TAAGCAGAGC CTTAATTTTA 1800
TTAGCCTGTT TATTAGCTCT GACCATGTGT TCAGAAAAAG TACCCTCAGC CTCTGAGTGA 1860
TCTAAGCCAG GCATAGTTCT CCTGTCTTCT TGTTGGTGAT TGGTTCTGGA AAAGGCTGGG 1920
ACACACTCCT GGCCAAGGAG AAGTCACAGC AGTGACTGAC TTGGAGGGGG AGTCTGCTGG 1980
GGGCTGGCTA GTGGAAGGCA TCTGGGGTAA AATGTTTTTG CTCTTAAAAA GTACTGTAGG 2040
AGGCCAGGCA TGTTGACTCA GGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGATGGGCAG 2100
ATCACTTGAG GTCAGGAGTT CGAGACCAGC CTGGACAACA TGATGAAACC CCATTTCTAT 2160
TTTTAAAAAT ACAAAAATTA GCTGGGCATG GTGGTGTGCA CCTGTAGTCC CAGCTACTCA 2220
GGAAGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGTTGCAGT GAGTGGACAT 2280
TGCACCACTA CACTCCAGCC TGGGTGACAG AGTGAGACTT CATCTCAAAA GAAAAAGAAA 2340
AGTACTGTAG GAGGCCAGGT GTGGTGGCTC ACACCTGTAA TCCCAGCATT TTGGGAGGCC 2400
AAGGCAGGAG GATCGCTTGA GCCCAGGAGT TCGAGACCAG CCTGAGCAAC ATAGCAAGAC 2460
CCCATCTCCA AAAAAATTTT AAAAAGATAC ACAAAATTTG CCAGGCGTGG CGGTGTGTGC 2520
CTGTATTCCT GGCTACTAAG GAAGCTGAGG AGGGAGAATC ACCTGAACCT GGGAGATCAA 2580
GGCTGCAGTG AGTCATAATC ACACCACTGC ACTCCAGCCT GTGTGACACA GCGAGATCCT 2640