EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-04392 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr10:105498320-105500790 
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:105500580-105500598CCTTCCTTCCTTCCCTTG-6.84
EWSR1-FLI1MA0149.1chr10:105500564-105500582CTTTCCTTCCTTCCACCC-7.24
EWSR1-FLI1MA0149.1chr10:105500576-105500594CCACCCTTCCTTCCTTCC-7.94
EWSR1-FLI1MA0149.1chr10:105500568-105500586CCTTCCTTCCACCCTTCC-8.03
EWSR1-FLI1MA0149.1chr10:105500572-105500590CCTTCCACCCTTCCTTCC-8.05
EWSR1-FLI1MA0149.1chr10:105500556-105500574CTTTCCTTCTTTCCTTCC-8.48
EWSR1-FLI1MA0149.1chr10:105500560-105500578CCTTCTTTCCTTCCTTCC-9.09
IRF9MA0653.1chr10:105498576-105498591AGTTTCACTTTTGTT-6.15
RREB1MA0073.1chr10:105500174-105500194CCCCAAACCAACCACAGCCT+7.82
TBPMA0108.2chr10:105499309-105499324GTATAAAAAGGGGGA+6.44
ZNF263MA0528.1chr10:105500584-105500605CCTTCCTTCCCTTGATCCACC-6.01
ZNF263MA0528.1chr10:105500556-105500577CTTTCCTTCTTTCCTTCCTTC-6.47
ZNF263MA0528.1chr10:105500572-105500593CCTTCCACCCTTCCTTCCTTC-6.51
ZNF263MA0528.1chr10:105500568-105500589CCTTCCTTCCACCCTTCCTTC-6.76
ZNF263MA0528.1chr10:105499206-105499227GGGGGAGAGAGGGAGGGAGAG+6.78
ZNF263MA0528.1chr10:105499822-105499843AGAGGAGGAAGGAGGAAAGGG+7.29
ZNF263MA0528.1chr10:105499214-105499235GAGGGAGGGAGAGAGGGAGGG+7.96
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_25254chr10:105498732-105499259Colon_Crypt_3
SE_26541chr10:105494553-105501529Esophagus
SE_27893chr10:105498846-105500161Fetal_Intestine
SE_32316chr10:105499231-105499973Gastric
SE_35962chr10:105498518-105500878HMEC
SE_50087chr10:105498702-105500946Sigmoid_Colon
SE_56459chr10:105497618-105500799u87
SE_64487chr10:105499033-105500263NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10105498744105499876
Number: 1             
IDChromosomeStartEnd
GH10I103737chr10105497715105501425
Enhancer Sequence
GGAAACCCAG GGGGACCACA GGAGGGTGGG GGAGGGCCCA CAAACCTGCA TGGAGCAGGG 60
CCTCAGCCTC CAAAAATGCA CTCCCGCCCT TTCTCATCCT GTTGGGGGAC AAAAAAGAAA 120
GCAGGGAGAT GGGAAGATAA ATGGGGTCCC TCTCCCAGCC CCCAATCTCA AGGTTAGCCA 180
AAGCTCTGGC TGAGGCTTAG ATCATTCCTG TCCTAGTTGC AGACAGAACT CTCTTTTTTT 240
TTTTTTCCCG AGACGGAGTT TCACTTTTGT TGTCCAGGCT GGAGTGCAAT GGCATGATCT 300
CAGCTCACTG CAGCCTCTGC CTCCCGGGTT CAAGCAATTC TCCTACTTCA GCCTCCCGAG 360
TAGCTGGGAT TACAGGCATG TGCCACCACA CCCGGCTGAT TTTGCATTTT TAGTAGAGTG 420
GGGTTTCTCC ATGTTGGTCA GGCTGGTCAC GAACTCCTGA CCTCAGATGA TCCGCCCACC 480
TTGGCCTCCC AAAGTGCTGG GAAGAACTCA TTTTAAAAAC TAGTTAAGGA GCACTGAGGC 540
CTCCACAGGT GTAGGAGATC CAGAGAAGGG AGGGATAGGT TGGGGTGGGG AGGTAGATGA 600
GAGGGTGCTC CTGACTCCTC CCCATGCTGG CCCCAAGCAC AGGACCCCGC CCTGCCCTCC 660
AGTCTGCACT CTGAGTGAGG CCACCGGGCC ACTGTGCCTG GGGCTGCCCA GTCCTCCCCA 720
CCAGGCTCCT GGATCTGCTG CTCACTTGCA AGGTCAGAGG AGAATTTCTG CACAAGCCAA 780
TTCCCAGCTG AGTTTTTGGA AGCCCAATGG GGCTTCCCCC TTTCCCGCTG AAATCCTGAC 840
AGGAGCAACG TTTTCTTTTC CCAGGGCTTT GGCACAATTG GCCAGTGGGG GAGAGAGGGA 900
GGGAGAGAGG GAGGGCCTGG AAGGGATTCT CCGGTCTTGA CTTCTCTGTT AGGAATCCAA 960
ACCACACTCT GAAAGCCAAA CCGGTGACCG TATAAAAAGG GGGAGAGAAA AAGGAGGGGG 1020
AGGAAAATCC CCATGAAGGA AGCCGGGACC ACAGGGCATT AAAGGCCTCT TGTAAATATA 1080
GTGCAGCCCG TTGACGGCAG GGCTCAGCTT CTGCCAGAGT CTTCAAAGCC ATCCAGATGC 1140
CGCCCTAGGA ATCTGATGAG CATCGCAAGG AAGATTGCAC GGGGCATGAG ACAGACCTAA 1200
CTCATCAGGA TTAACTCAGT CCTGAAAGCG GAGAAGAAGC TGTGCAGCTG CGACGTCTAA 1260
GCAGTAACTG GAGGTCCTTC TTCCTGCCAC TCTGGGCTGG GCTGGGGTGA GACCAGCGAA 1320
GGAGTGGGGG CCTCCGGTGG GAGTCTGGGG TTCAAGTCCT ACCTGGGCCA CAGGCTGGCT 1380
GTGTGACCCT GAAACAGGTC CCTTCTCCAC TGGGACTGCT GTGTGCTCAT CGGAGGCCTG 1440
GGCTCTATGG CTGCTACCTC TGGAAGCCCT AAGATTGATT GACAGTGGGG ACGTTAGTGG 1500
GCAGAGGAGG AAGGAGGAAA GGGTTAATGG TAGCTAAGCG CTCAGCACAC ACCTGGTGCA 1560
CACTAAGAGC TTTTCACTGA ATTCCCTCCC TTCATCCTCG CAACAACCTT GAAGCAAGTA 1620
CTTTAACCAG GCCCATTTTG TCCTAGAGGA GATGGCAGCT CAGAAAGGTT GAAGGACCTG 1680
TCCAAAGTCA CACAGCTATC TAGTGGCTGA GCTGGGATTT CAACCTGGGG TTTTAAAGCT 1740
TAGAGAGTGT GGGGGAGCCA TGATCTTTGC ACTTGGATCA TGTCAAGCCT TGAGAGCCAC 1800
CGTGAGGACT TTGGATTTTA TTCTGCATGT GAAGGGAGAT GAGAACAGTT AAACCCCCAA 1860
ACCAACCACA GCCTCCAGGG CTCTTCTTGG GAAAGCGGTA CCTATGGGAT GGACTCCCAT 1920
GAGAGCCAGG GCCTGGGGCC TCAAGTAGAA TCACCAGACA CAGTACCACT GGCCAGGGTC 1980
CCCACACCAG CCATGAAGAG TTTGGTAGCT ACCTCCATGA ACTAGGACCC ATTTGTAGAG 2040
GTAATAAGAG GGCACTGATT ATAGGAGCCG TAAGAGAGGG CTGGCCTCGG GACCTCTTCT 2100
GGTCTGAGCA GGCTGATCTA TTCCTGGCAG CCTCTCCTCT TCACACTCAC AGTGTCTATG 2160
CATGCATGTA CAACTCCTTT TTCCCTGTCT TTCTGCCACT TGGAACGCCA TTCATTCTTG 2220
GAAGACTTCC CCCTGCCTTT CCTTCTTTCC TTCCTTCCAC CCTTCCTTCC TTCCCTTGAT 2280
CCACCCAGCA CTGTCTTGAT GGAGGCCTGC TGTGCTGGGC TCTGTTCCAG GCGCTGGGAG 2340
CACAGCAGTG AACCAGACAG ATGAGGGCCT TGCTCTCAGG AGTTTACCTT CCAATTGGGA 2400
AGGGAGTGGG CACGGGAAGA AGGCAGTACA CATTTTCATA CCTATTGAGT AATTTGGTTA 2460
TACTTCCAGG 2470