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

TagContent
EnhancerAtlas ID
HS012-01390 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr10:31421710-31424420 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1776631chr1031422577hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB3MA0638.1chr10:31422761-31422775GCGCCACGTCACCC+6.07
EWSR1-FLI1MA0149.1chr10:31421974-31421992ACATCCTCCCTCCCTTCC-6.3
EWSR1-FLI1MA0149.1chr10:31422196-31422214GGAAAGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr10:31421982-31422000CCTCCCTTCCTCCCTCCC-6.88
EWSR1-FLI1MA0149.1chr10:31421978-31421996CCTCCCTCCCTTCCTCCC-6.92
EWSR1-FLI1MA0149.1chr10:31422192-31422210GAAAGGAAAGGAGGAAGG+7.05
EWSR1-FLI1MA0149.1chr10:31422204-31422222GGAAGGGAGGGAGGGAGG+7.08
LMX1BMA0703.2chr10:31423921-31423932AATTTAATTAA+6.32
MEOX2MA0706.1chr10:31422236-31422246AGTAATTAAC+6.02
Nr2f6(var.2)MA0728.1chr10:31424180-31424195AAGTTCAAAAGTTCA+6.19
Nr2f6MA0677.1chr10:31423949-31423963CAGGTCAAAGGTCC+6.05
RARAMA0729.1chr10:31424180-31424198AAGTTCAAAAGTTCATAT+6.18
RxraMA0512.2chr10:31424173-31424187AAGGTTAAAGTTCA+6.18
ZNF263MA0528.1chr10:31421974-31421995ACATCCTCCCTCCCTTCCTCC-6.09
ZNF263MA0528.1chr10:31422888-31422909CCCCTCCTCGCCCCCTCCCCC-6.36
ZNF263MA0528.1chr10:31422202-31422223GAGGAAGGGAGGGAGGGAGGA+6.63
ZNF263MA0528.1chr10:31421981-31422002CCCTCCCTTCCTCCCTCCCCA-6.85
ZNF263MA0528.1chr10:31422210-31422231GAGGGAGGGAGGAAAAGAGGG+7.25
ZNF263MA0528.1chr10:31422201-31422222GGAGGAAGGGAGGGAGGGAGG+7.9
ZNF263MA0528.1chr10:31422198-31422219AAAGGAGGAAGGGAGGGAGGG+8.12
ZNF263MA0528.1chr10:31421977-31421998TCCTCCCTCCCTTCCTCCCTC-8.35
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_25423chr10:31420765-31433717DND41
SE_30759chr10:31421649-31424498Fetal_Muscle
SE_39587chr10:31421494-31430224Jurkat
SE_66545chr10:31421494-31430224Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr103142360031424302
Number: 1             
IDChromosomeStartEnd
GH10I031132chr103142154631427344
Enhancer Sequence
CTCACGAAAC TTACAGTCCG GTGGGGAGGG TGAATTTTGC CCGGTTGTAC ATTTGATGAG 60
TATTACAAAA GAGAAGATGA AAGAGCTACA GGATCCTGTA ACTGGAGGAC CTGATCTGGC 120
CCAGGCACCA GGGAAGTGAC ATTTCACCTG AGGCCAGAGG AATAAGTGGG AGGGGAATGG 180
GCTGGGGGTG GGCTATGCAG GGAGACCTAT GTGGGCAAAG GGCCTTTCTC CTGGTAAGTT 240
TCTACTCACC CAGCCTCCAC CTGGACATCC TCCCTCCCTT CCTCCCTCCC CAGGAGCTGG 300
GCTGAGGGCC GCCCTACTGC TATCCATGGC ACTTGTCACC CAGAGCCCTG GTGAACTGTT 360
TGCTTGTATG CAGCACCCCT CACCACATGA AGAGCATCTC AAGGGCTAGG AGTCTCGTTT 420
CTTGTATCCC TGGTCCACCG CCTGATCTCC AGCACACATG AGGTATCCAT CAAAATGTTA 480
GCGAAAGGAA AGGAGGAAGG GAGGGAGGGA GGAAAAGAGG GAACAAAGTA ATTAACGAAT 540
CCCTAGCTGC AGGCACAGGT TGATTCTCTG CAATGTCTCC TTTTCTGTCA CAGAGAAAAA 600
GAGCACAGTT AGAGTTCACA GGGACCGCGC CCTGCCACAC ATTAATTTAT TCTCCAAACA 660
TTTGTGGAAG TTGCTAGAGA CACAGATGCA ACGTGTTTTC AGGGAGCTTA TGATCTAGCA 720
GTGGAAGCGC AACAGAAGTG CAATTCTTTC ATCCTTTTGC CCACATAAAG CAGGCAAGGC 780
ACGACGAATT TTGATGTCAA CTGCCCAGGC AGGACTTTGT CCCAGCCCAG CGACCCTCAC 840
GAGGCCAAGG GCAGAGATGA TAGTTGTAAT ATACTCTTCT GTCCATTTCC TTGATATTCT 900
CCTCAAGGGG TGGGGGGCGC CTGAAATCCA TCTGCCCCGG GGAGAAGGGC CTCGTGGGCC 960
AGCGCAGCTT GCTCCTCTGC AGACCCAGAA GCATTTGTGC GTCCCGGGCG TGGCAGGCCC 1020
GGCGCCCACT CCGCCCTCCC GCCCCTCCCC CGCGCCACGT CACCCGGGTC ACGTGAGTGA 1080
CCAGGCTCCT CACCCCAACC CCCCTCCCTA CTCCCGCCAG ACTCAGCTGC TCTCCCCGGG 1140
AGCTGGGGAG CCGGGGGCGG GCAGCCGCGT CTGTCCTGCC CCTCCTCGCC CCCTCCCCCG 1200
CAGCCTGAGG AGGGCGTTAA GCAAGGGGCT TCGGAGAAAT TAGAACCAGC GTTCTAAATT 1260
AAGGGGAGCA GATGTCCTTG TTTTGCTCGC GAGGCCTGGG TGGCCTGCTG TTCAGACAGA 1320
AATCGTTGAG GCGCTGACCT TCCGGGACTG CTGTCAATCT CCGCGTGCAG ATGGCCAGCC 1380
CGGAGCCTCG CCGCTCCCCT GCATTGGAAA TGCGGCAGCC GGGGGTGCCG GCAGCTTGAG 1440
AGAAAAGTCT GCGTGGAGGG GGGGTGGGGG GGATGAGGGG AGGCCCGGGG AGACAGAGGG 1500
CAGGAGAAAA AGGCCGGCCC CGCTCACAAT GGAGCCCCTG TGGCGGCCCC TCCGAGACAA 1560
TGCGGTCCCC CGGGACCCGC GGTGGGTTGC GCCAGGCCAG TCCGCGCTCC AGCTGCCTCT 1620
TCAGAACAAG GCAGTGCAAA TGTGCCCACT TGATTCTAAA TCCTCTTAGG CGCTGTCCAT 1680
GTGAACAAGG AAAGGGGTGG CCCTACGATC CTTTACAATC GGAGGCCTGG GGAGGCCTGG 1740
GAGCCCTGGA GCTCCGGAAA ATGTCTGCAC CACGCATGCA AATGGGTCAT TTCGCTTGGA 1800
GAGAGGCATC TGGCGACATC GGCAGAAAGG CTCTCTGCCC GGTAGACGGT GAACAAAACC 1860
CACAAAACCA GCCAGCCAAC AGCGTGCACT AAACACCCCT CTCTGGCCCT TCAATGCCAC 1920
CCGGAGTCCT GAAACATTTT CAGGTTGTTT CCCCTGGAGA GACGTCCCAT GAAATGTTCA 1980
GAAAAGCCAG CTGAGCTGTG CAAAGTCATT AGTCACCCAG GTATTTACAC TGTTTTTCCT 2040
ATTTCCTTTC TCTTTTGGCC TCTGTGGTCA GTGGTATAAA ATTCCTAGGA ACTCCCACCT 2100
AAACACCAGC TTCCTGTTTA TTCTTGCAGT GGCTTTAATG TTTCGCTGTT AAAAGCGGTT 2160
GACCAAGACA CTGAAACAAT CAGTAGAGGT TCGCAGGTGA ATGGAAAAAA AAATTTAATT 2220
AAAAAATATA TCTACTGCTC AGGTCAAAGG TCCAGGTTCA TTTTTACTGC TTATGTCAGA 2280
ATCGCAAAGG GGAAAAGGTA AAATTAAAAT GTAACTTAAT GCCTAAGATC TTGGTTCAGT 2340
TTCATTTGGC CCCTGTGTCT ACATGAACCT ATAAAATACG ATACACTAAA GTATGAATGT 2400
TTTCATTTCT AGCAGTGGAA GGCCTTTTTT TTTTCAATGT GGCATGACGT TCTTTTGTTA 2460
GAGAAGGTTA AAGTTCAAAA GTTCATATAT TAGCACAATC TGTGTGCTCC TGCGTGTGCC 2520
TTACACCTCG CTATGCCTGT TCCGCCTTAA TTTCCTGCAG CAAAACCTTG CATTTACAGA 2580
GCCATCAGAA TTGCAGCCTC CCTGGCCTGG AAAAGAACCC TCGAAGTCAC CTCATTCAAC 2640
CCTTTTCCAA TACTGAATTC CCTGTATGGC CCCTAGGGAG TGTTAGTGAT GGGACCCTTT 2700
CTACCTCAGA 2710