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

TagContent
EnhancerAtlas ID
HS001-01154 
Organism
Homo sapiens 
Tissue/cell
786-O 
Coordinate
chr10:31421530-31424600 
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
AACCACAGCC CCTTGGTACC AGGCAGTTCC CACTGGTACT CGGAGTGGAG CCGTCACAGC 60
TTGTCCTGGC ATCCCAAACA GAAAATGTAT GTATGGATTT CTCACTAACT TAAGAGGAGT 120
CTGACTATTC ATTGGCTCAA CAAGTATTTA TGGGGCATGA GGAGTCAGGC ACAGTGCTGG 180
CTCACGAAAC TTACAGTCCG GTGGGGAGGG TGAATTTTGC CCGGTTGTAC ATTTGATGAG 240
TATTACAAAA GAGAAGATGA AAGAGCTACA GGATCCTGTA ACTGGAGGAC CTGATCTGGC 300
CCAGGCACCA GGGAAGTGAC ATTTCACCTG AGGCCAGAGG AATAAGTGGG AGGGGAATGG 360
GCTGGGGGTG GGCTATGCAG GGAGACCTAT GTGGGCAAAG GGCCTTTCTC CTGGTAAGTT 420
TCTACTCACC CAGCCTCCAC CTGGACATCC TCCCTCCCTT CCTCCCTCCC CAGGAGCTGG 480
GCTGAGGGCC GCCCTACTGC TATCCATGGC ACTTGTCACC CAGAGCCCTG GTGAACTGTT 540
TGCTTGTATG CAGCACCCCT CACCACATGA AGAGCATCTC AAGGGCTAGG AGTCTCGTTT 600
CTTGTATCCC TGGTCCACCG CCTGATCTCC AGCACACATG AGGTATCCAT CAAAATGTTA 660
GCGAAAGGAA AGGAGGAAGG GAGGGAGGGA GGAAAAGAGG GAACAAAGTA ATTAACGAAT 720
CCCTAGCTGC AGGCACAGGT TGATTCTCTG CAATGTCTCC TTTTCTGTCA CAGAGAAAAA 780
GAGCACAGTT AGAGTTCACA GGGACCGCGC CCTGCCACAC ATTAATTTAT TCTCCAAACA 840
TTTGTGGAAG TTGCTAGAGA CACAGATGCA ACGTGTTTTC AGGGAGCTTA TGATCTAGCA 900
GTGGAAGCGC AACAGAAGTG CAATTCTTTC ATCCTTTTGC CCACATAAAG CAGGCAAGGC 960
ACGACGAATT TTGATGTCAA CTGCCCAGGC AGGACTTTGT CCCAGCCCAG CGACCCTCAC 1020
GAGGCCAAGG GCAGAGATGA TAGTTGTAAT ATACTCTTCT GTCCATTTCC TTGATATTCT 1080
CCTCAAGGGG TGGGGGGCGC CTGAAATCCA TCTGCCCCGG GGAGAAGGGC CTCGTGGGCC 1140
AGCGCAGCTT GCTCCTCTGC AGACCCAGAA GCATTTGTGC GTCCCGGGCG TGGCAGGCCC 1200
GGCGCCCACT CCGCCCTCCC GCCCCTCCCC CGCGCCACGT CACCCGGGTC ACGTGAGTGA 1260
CCAGGCTCCT CACCCCAACC CCCCTCCCTA CTCCCGCCAG ACTCAGCTGC TCTCCCCGGG 1320
AGCTGGGGAG CCGGGGGCGG GCAGCCGCGT CTGTCCTGCC CCTCCTCGCC CCCTCCCCCG 1380
CAGCCTGAGG AGGGCGTTAA GCAAGGGGCT TCGGAGAAAT TAGAACCAGC GTTCTAAATT 1440
AAGGGGAGCA GATGTCCTTG TTTTGCTCGC GAGGCCTGGG TGGCCTGCTG TTCAGACAGA 1500
AATCGTTGAG GCGCTGACCT TCCGGGACTG CTGTCAATCT CCGCGTGCAG ATGGCCAGCC 1560
CGGAGCCTCG CCGCTCCCCT GCATTGGAAA TGCGGCAGCC GGGGGTGCCG GCAGCTTGAG 1620
AGAAAAGTCT GCGTGGAGGG GGGGTGGGGG GGATGAGGGG AGGCCCGGGG AGACAGAGGG 1680
CAGGAGAAAA AGGCCGGCCC CGCTCACAAT GGAGCCCCTG TGGCGGCCCC TCCGAGACAA 1740
TGCGGTCCCC CGGGACCCGC GGTGGGTTGC GCCAGGCCAG TCCGCGCTCC AGCTGCCTCT 1800
TCAGAACAAG GCAGTGCAAA TGTGCCCACT TGATTCTAAA TCCTCTTAGG CGCTGTCCAT 1860
GTGAACAAGG AAAGGGGTGG CCCTACGATC CTTTACAATC GGAGGCCTGG GGAGGCCTGG 1920
GAGCCCTGGA GCTCCGGAAA ATGTCTGCAC CACGCATGCA AATGGGTCAT TTCGCTTGGA 1980
GAGAGGCATC TGGCGACATC GGCAGAAAGG CTCTCTGCCC GGTAGACGGT GAACAAAACC 2040
CACAAAACCA GCCAGCCAAC AGCGTGCACT AAACACCCCT CTCTGGCCCT TCAATGCCAC 2100
CCGGAGTCCT GAAACATTTT CAGGTTGTTT CCCCTGGAGA GACGTCCCAT GAAATGTTCA 2160
GAAAAGCCAG CTGAGCTGTG CAAAGTCATT AGTCACCCAG GTATTTACAC TGTTTTTCCT 2220
ATTTCCTTTC TCTTTTGGCC TCTGTGGTCA GTGGTATAAA ATTCCTAGGA ACTCCCACCT 2280
AAACACCAGC TTCCTGTTTA TTCTTGCAGT GGCTTTAATG TTTCGCTGTT AAAAGCGGTT 2340
GACCAAGACA CTGAAACAAT CAGTAGAGGT TCGCAGGTGA ATGGAAAAAA AAATTTAATT 2400
AAAAAATATA TCTACTGCTC AGGTCAAAGG TCCAGGTTCA TTTTTACTGC TTATGTCAGA 2460
ATCGCAAAGG GGAAAAGGTA AAATTAAAAT GTAACTTAAT GCCTAAGATC TTGGTTCAGT 2520
TTCATTTGGC CCCTGTGTCT ACATGAACCT ATAAAATACG ATACACTAAA GTATGAATGT 2580
TTTCATTTCT AGCAGTGGAA GGCCTTTTTT TTTTCAATGT GGCATGACGT TCTTTTGTTA 2640
GAGAAGGTTA AAGTTCAAAA GTTCATATAT TAGCACAATC TGTGTGCTCC TGCGTGTGCC 2700
TTACACCTCG CTATGCCTGT TCCGCCTTAA TTTCCTGCAG CAAAACCTTG CATTTACAGA 2760
GCCATCAGAA TTGCAGCCTC CCTGGCCTGG AAAAGAACCC TCGAAGTCAC CTCATTCAAC 2820
CCTTTTCCAA TACTGAATTC CCTGTATGGC CCCTAGGGAG TGTTAGTGAT GGGACCCTTT 2880
CTACCTCAGA TTTTATAAAT TTATTTTTTA GAGACAAGGA TCCACTCTCT CGCCCAGGCT 2940
GGAGTGCAGT AGTACCATCA CAGCTCACTG CAGTCTCTAA CTCCTGGGCT CAAGTGGATC 3000
CTCCCACCTC AGCCTATGAG TAGCTGGGAC TACAGGCATG TGCCACCATA CCTGGCTAAT 3060
TTTTTAAATT 3070