EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-00043 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr1:1003500-1006350 
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: 3             
ChromosomeStartEnd
chr110052931005547
chr110060441006328
chr110036001006245
Number: 1             
IDChromosomeStartEnd
GH01I001066chr110018371006486
Enhancer Sequence
CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC 60
CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC 120
CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG 180
GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC 240
CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC 300
CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT 360
CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC 420
CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG 480
CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC 540
GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG 600
GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG 660
GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG 720
AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG 780
GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC 840
ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT 900
GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA 960
GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC 1020
AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT 1080
GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA 1140
GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG 1200
GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC 1260
GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT 1320
CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG 1380
CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG 1440
GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC 1500
TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC 1560
CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA 1620
GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC 1680
GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG 1740
GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT 1800
GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG 1860
TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG 1920
GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG 1980
TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC 2040
TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG 2100
CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC 2160
AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG 2220
ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG 2280
ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC 2340
TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC 2400
TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT 2460
CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG 2520
GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC 2580
AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC 2640
ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG 2700
TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC CTGTCCCAGT 2760
GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC 2820
CCAGGGTGAG GCCCTCTTGC CAAAGATGGA 2850