EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS003-00023 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr1:1003830-1006910 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3934834chr11005806hg19
TF binding sites/motifs
Number: 19             
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
NKX2-5MA0063.2chr1:1006876-1006886CTCAAGTGGT-6.02
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
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
TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG 60
AAACCCAGCT GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC 120
GCTCAGGAGG AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC 180
GGCGTCCGGG CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG 240
AGCAGCAAGC CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA 300
CGCGGGCTGT GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG 360
TGCGGCGGGG CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC 420
CCCCGCCCCC GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC 480
GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC 540
GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA 600
CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC 660
CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC 720
CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT 780
CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC 840
GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG 900
CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC 960
GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC 1020
GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC 1080
GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC 1140
CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC 1200
CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA 1260
GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT 1320
CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG 1380
CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC 1440
GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC 1500
ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG 1560
CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG 1620
TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA 1680
CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG 1740
GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA 1800
CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT 1860
GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG 1920
CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC 1980
CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG 2040
AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG 2100
TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG 2160
CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG 2220
CCCCCTTTGT CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG 2280
CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT 2340
CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC 2400
CCCTAGAACC TTGGGCCCAC CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA 2460
TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA 2520
TACAAATAAT TTATTTTAAA AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC 2580
TGTGGTTACC TTGCACTGGG GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC 2640
AAGATGAGCA CCCCCACCCA ATGGCAGGAC CAGCCCTGCG GGGAAATGTC AGCATGAGTG 2700
GAAGCACGGC AAGGCCCCTT CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC AGTTCACAGG 2760
GTGTGTGGGT GGGGGGGATG CTGACCAGCT GCTCTCCTGG ACCCTTCCTG TACGAGCCTG 2820
TTTTTTTTTG TTTTGTTTTG AGACAGGGTC TCCCTCTGTC GCCCAGGCTG GATGCAGTGG 2880
TGCAATCTTG GCTCACTGCC ACCTCCACCT CCCCGGTTCA AGCAGTTCTC CTGCCTCAGC 2940
CTCCCCAGTA GCTAAGAGGC ACCCACCACG ATGCCCGGTT AATTTTTGTA TTTTTAGTAG 3000
AGATGGGGTT TCACCATGTT GGCCAGGCTG GTGTCAAAAT CCCGACCTCA AGTGGTCTTT 3060
CTGCCTCAGC CCTCCAGAGT 3080