EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS080-00022 
Organism
Homo sapiens 
Tissue/cell
H9 
Coordinate
chr1:1003160-1006230 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3934834chr11005806hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr1:1004737-1004751GTGGGGGCGTGGCC-6.39
KLF16MA0741.1chr1:1004739-1004750GGGGGCGTGGC-6.62
KLF5MA0599.1chr1:1004502-1004512GCCCCGCCCC+6.02
KLF5MA0599.1chr1:1004521-1004531GCCCCGCCCC+6.02
KLF5MA0599.1chr1:1004157-1004167GGGGCGGGGC-6.02
KLF5MA0599.1chr1:1004196-1004206GGGGCGGGGC-6.02
Klf1MA0493.1chr1:1005572-1005583TGGGTGTGGCC-6.62
NRF1MA0506.1chr1:1004721-1004732GCGCCTGCGCG+6.14
RFX1MA0509.2chr1:1004774-1004790CGTCGCCATGGTGACC+6.11
RFX1MA0509.2chr1:1004774-1004790CGTCGCCATGGTGACC-6.12
RFX2MA0600.2chr1:1004774-1004790CGTCGCCATGGTGACC+6.2
RFX2MA0600.2chr1:1004774-1004790CGTCGCCATGGTGACC-6.2
SP1MA0079.4chr1:1004499-1004514CAAGCCCCGCCCCTC+6.34
SP2MA0516.2chr1:1004498-1004515GCAAGCCCCGCCCCTCA+6.23
SP3MA0746.2chr1:1004738-1004751TGGGGGCGTGGCC-6.57
SP4MA0685.1chr1:1004499-1004516CAAGCCCCGCCCCTCAT+6.24
SP8MA0747.1chr1:1004738-1004750TGGGGGCGTGGC-6.11
ZNF263MA0528.1chr1:1003831-1003852CCTTCCTCCTCCTCCTGCTCG-6.88
ZNF263MA0528.1chr1:1003819-1003840CCCTCCCCATTTCCTTCCTCC-6.89
ZNF263MA0528.1chr1:1003825-1003846CCATTTCCTTCCTCCTCCTCC-7.03
ZNF263MA0528.1chr1:1003822-1003843TCCCCATTTCCTTCCTCCTCC-8.3
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_24070chr1:1002554-1005867Colon_Crypt_2
SE_24817chr1:1002490-1006081Colon_Crypt_3
SE_27529chr1:1001798-1011077Esophagus
SE_34539chr1:1002321-1004360HCT-116
SE_34539chr1:1004454-1006480HCT-116
SE_41944chr1:1001963-1005965LNCaP
SE_58139chr1:1003761-1004209VACO_9m
SE_58139chr1:1004236-1004768VACO_9m
SE_58139chr1:1004812-1005267VACO_9m
SE_65935chr1:1001682-1006445Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr110034591003600
chr110052931005547
Number: 1             
IDChromosomeStartEnd
GH01I001066chr110018371006486
Enhancer Sequence
TGGCTGCACG TACACACCTG CGTCTCTGCA GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC 60
CAGCAAGGCT GATGCAAAGC GCTCCCCTCG GAACAAGTGT TTCCGGGACT GGCCAGAGCT 120
GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA CATGCGCGTC CTCGGCAAGG GCCAGGCCCA 180
GGGCTACTGC GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT 240
GGAGCGTGCC TGCTGTCGGC CTGCACTGGG AGACCCCACA CCTGCCTGCA TCCAACCCCA 300
CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG CATTCCAAGC CTGGACAGGG 360
GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC CGCTCCTCCC ACACACCTCT 420
CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC CATTTCTGCT CCGGGCAGAT 480
TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT 540
GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG 600
CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC 660
CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG 720
GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC 780
CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG 840
GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA 900
CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG 960
GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG 1020
CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG 1080
GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG 1140
TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG 1200
CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC 1260
CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG 1320
ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG 1380
GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG 1440
ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA 1500
CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC 1560
TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC 1620
CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA 1680
CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG 1740
TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC 1800
AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA 1860
CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG 1920
TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC 1980
TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG 2040
TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT 2100
CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC 2160
CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC 2220
ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA 2280
TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA 2340
CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC 2400
CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA 2460
GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG 2520
GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG 2580
GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG 2640
GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC 2700
TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT 2760
TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG 2820
GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG 2880
AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG 2940
GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC 3000
ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG 3060
GAGTTGGACC 3070