EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS059-00020 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr1:1003670-1006640 
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
chr110052931005547
chr110060441006328
Number: 1             
IDChromosomeStartEnd
GH01I001066chr110018371006486
Enhancer Sequence
TGTGTGTGGG GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA 60
AATAACTGTC CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA 120
CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT 180
CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC 240
CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG 300
TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC 360
CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG 420
GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG 480
GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG 540
CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT 600
CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT 660
CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC 720
CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC 780
CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC 840
CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC 900
AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG 960
TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG 1020
CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC 1080
CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG 1140
CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG 1200
CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC 1260
CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC 1320
CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG 1380
CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT 1440
CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC 1500
GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC 1560
ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG 1620
TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA 1680
GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC 1740
CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG 1800
CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT 1860
GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG 1920
CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC 1980
TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG 2040
CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT 2100
GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT 2160
AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG 2220
ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT 2280
CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG 2340
GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG 2400
GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG 2460
GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC 2520
CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC 2580
CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA 2640
GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA 2700
AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC TGTGGTTACC TTGCACTGGG 2760
GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC AAGATGAGCA CCCCCACCCA 2820
ATGGCAGGAC CAGCCCTGCG GGGAAATGTC AGCATGAGTG GAAGCACGGC AAGGCCCCTT 2880
CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC AGTTCACAGG GTGTGTGGGT GGGGGGGATG 2940
CTGACCAGCT GCTCTCCTGG ACCCTTCCTG 2970