EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-00022 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr1:1001930-1006610 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3934834chr11005806hg19
TF binding sites/motifs
Number: 22             
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
Pou2f3MA0627.1chr1:1002525-1002541TATCATTTGCATAGCA-6.09
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: 8             
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_58139chr1:1004236-1004768VACO_9m
SE_65935chr1:1001682-1006445Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr110034591003600
chr110052931005547
chr110060441006328
chr110036001006245
Number: 1             
IDChromosomeStartEnd
GH01I001066chr110018371006486
Enhancer Sequence
TGAAGGCTCC ATCACCTCCA GATGCTGCAG CAGCAGGAAT GCCGGTTCCT GTACCCTCGG 60
AAGGAGGGGC AGAGTGTGGA GAACAAGCCC AAGAATCACT ACAAGAACAT CCTTCCCTGT 120
GAGGGCGGAG GCCAGGGCGT CACCCGTCGG GCCTGGGGGA GGTGGGGGGC AGGCCGAGCA 180
TCTGCCACCG CTGACCTGAG GCTCCCCCTT GCATACCCTG GACCCTCCAT CTCTGCTCAC 240
CACAGGGTCT GCGGGCAAAG AGGCAGGGTG AGGCCCACGA GCTGTGCCCT GGAGAACTGA 300
GCGGCACCTC CCTTCCCAGT TGATGCTACC CTTGAGTCAT CCTGCTCAAC GAGGATGACA 360
GCGGGCCCGG AGCCGACTAC ATCAGGGTGG GTGTGTGCGG GAGGCGGGGC CTGGGCCCAT 420
TGCTCCTGGG GGGCTCAGGA AGAACCAGGG TCCCCAAGGG AGGGGTGGGC GGCAGTCTCC 480
AAGGGGTCCT CAGAGAGGCT GGACGGGCAT TGGTCCTCAG CCCCTTGCTG GCCTGGAGTG 540
AGGAGTGTGT TTAAGCCACC AGGGCTCTTT GCATAATATT TGTGTGTCGT TTGCATATCA 600
TTTGCATAGC ATTTGCATGG ACTTGTTTGT CCTCTGTTAA CAGCAGCAGT TGGCCTCATT 660
CCCTTTCAGA CTGACCCTGA GGAGGAGCCG GGCCATGGCA GGGGCAGGGT GGACATCCCT 720
TGTGGCCCTG CCCCGCCGCA CCTGCACCTG CACAGCCCGC GTGGGCCCGC CCCGCCGCAG 780
CTGAAGTGCA CCACCATGGG CCCGGCCCGC GGCTCGCGGC TCGCGGCTCT GGGCCCGGTT 840
CACCTCGTCC CGGAAGCCGA GGACGCCGGC GGGATCGGTC CGGACGCCGT AGTCCGGCCA 900
GCCGAAGTAC TGGAAGTGCT GCACCGTACG CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC 960
GCGGGCGCAG GGTGTACATC GCCTGCAGGG CTGTCTGCAG GCCTGTCTGC AGGCCACGGT 1020
GGCTGCTTTC TGGGCCACGG TGCACCAGGA GAACACGCGT GTCATCGTCA TGACCACCAG 1080
GGAGATGGAG CGGGGCCGGG TAGGGGTGCG GTGCCAGTGC TCCCAGTGCC CATCCCACCC 1140
CGTGCATCTT CGGCTGCCCA AGGCCCTTCC CGACCAGGCC AAGGAGGCTG TGGGACGCCG 1200
TGGGAGTGGG GAGGCTCCCA CAGAGCCCCG TGGCTGCACG TACACACCTG CGTCTCTGCA 1260
GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC CAGCAAGGCT GATGCAAAGC GCTCCCCTCG 1320
GAACAAGTGT TTCCGGGACT GGCCAGAGCT GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA 1380
CATGCGCGTC CTCGGCAAGG GCCAGGCCCA GGGCTACTGC GTGCGGGAGC TGCAGGTGTG 1440
GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT GGAGCGTGCC TGCTGTCGGC CTGCACTGGG 1500
AGACCCCACA CCTGCCTGCA TCCAACCCCA CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC 1560
CCAGGAGGTG CATTCCAAGC CTGGACAGGG GTCACTGACG TGGCCACATT CTCAGCCCTG 1620
GGCTGGCGGC CGCTCCTCCC ACACACCTCT CCAACTGCAG CTTTGGTCTC CGTTGTATAC 1680
CAGAGACGCC CATTTCTGCT CCGGGCAGAT TACCTCGTGT TCCCTCCAGC CCCCGCCCAG 1740
TGTGTGTGGG GGGGTCCTCC AGGACCCCAT GGACCCCTCA CATTTGGTTT TTCCTTATAA 1800
AATAACTGTC CTCACAGCCT GCTTCGCCCG CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA 1860
CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC CCTCCCCATT TCCTTCCTCC TCCTCCTGCT 1920
CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG GCACTCCCGG AAACCCAGCT GTGCCTCAGC 1980
CTCCTCCTCC CACCCTGGGG TCACACTCAC CGCTTGCCCC GCTCAGGAGG AGCCACAGCG 2040
TACGGTGCAG CACTTCCAGT ACTTCGGCTG GCCGGACTAC GGCGTCCGGG CCGATCCCGC 2100
CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG 2160
GCCCATGGTG GTGCACTTCA GCTGCGGCGG GGCGGGCCCA CGCGGGCTGT GCAGATGCAG 2220
GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG CAGGTGCAGG TGCGGCGGGG CGGGGCCACG 2280
CGGGACGACG AGGGCGGAGC CATCGGGTGG GCGGGGGCGC CCCCGCCCCC GCCCCCCACT 2340
CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG TGGGGGCATC GGATGCACGG GCACCATCAT 2400
CGTGATTGAC ATCCTGGTGG ACGTCATCCG CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC 2460
CCCCCGCCCT GCCCTGCTAT AGCCCCACCC CTCCGGGCGA CCCCACCCCT CCGGACGACC 2520
CCACCCCTCA GGACGACCCC ACCCCTCAGG ACGACCCCAC CGCTACCGGC AAGCCCCGCC 2580
CCTCATCAGC AGCCCCGCCC CTGCCTGCCG GCACCTTCCC CCCATCCGTA GCCCCTCCCC 2640
AAGCGCGCTT GTCCGCAGGG CTGGACTGCG ACACCGACGT CCCGAAGACG ATCCAGCTGG 2700
TTTGGCGGCA GCACTGGGGA ATGGTGCAGA CGGAGGCTCC GTACAAGTTC ACGTACCTGG 2760
CGCTGCAGCG GCACATCCGG GGCGAGTAAC TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC 2820
CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC CATGGTGACC GGCGGCCCCT CCCCCCAGCG 2880
CGAGCCGCCT CAGGAGCGCG AGAACCAAAA CGTGGGCGCC GCCCCCCGCT AATCGGGTTG 2940
CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC 3000
CTCTGGGAGG GACTGGGACG TGCGGGGTGC AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC 3060
CCCGCAGCCC TGGGACGGCG AGGACGCGAA CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG 3120
CAGGGAACCC CCGGCCTAGC CGCGCCCGCG TGTGGCCGGA GCTGCGGGCC GGGACTGTGT 3180
CCAGGACAGA GCCACAAGCT TGTCCCCAGC TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC 3240
GACAGGCTGC GAAGCCCACC GGTGACCACG TGTGAACCCG CGTGCGCCCC CAGCTCGGCC 3300
ACTCCGTGCG GGTCTGCCCT CACCGCAGCT CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG 3360
TCTGGGATGT GGCCCCGGTG AGGACCCGGC CCCATCAGGC ACAGGGTGGA TGTCTGTGGA 3420
GTGAGGTGTG TGTGACATAT TCATGTGACC ACCCGTGCAG CGTCACGCGC CTGGCCCTGC 3480
CGATGACAAG GGTGTGGGCC TGCGTGGGCA TGACTGTGTG TGTGACACAG AGTGATGTTG 3540
CTGTGACCCG TGGCTGCACT CCCCACATCA CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT 3600
GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC CTGGGGCAAG GGTGGGTGTG GCCCCCACAG 3660
CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA GCCCTCCCCA CCCTGGACCA GAGGCCCAGC 3720
TGGTTGGAGC AGGAAGTACC TGGGCTCTGG GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG 3780
CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG GCCGTGCCTG CCTGGTGGTG CAGGATTCCT 3840
GGGGCTGATG ACAGACGGGG TAGGGCTGGG GTTGGCGAGC CTCCTGCCGA TACCTCACGT 3900
AGCTGACCTC TGACTCTTCC CCAGCCAGGC TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG 3960
ATCTGCAGGC TGCACGCTGG CTGTTACCTT TGCTTCTGGG TTCCCACAGG GGTCATGGTT 4020
CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG GGCCATGGGG CGTGACTTCC TGGAGGTGTG 4080
GCCTAGTATG GCCACGGCAG AGGATGGGGG AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG 4140
GCTCTGAACC AAGCTGAAGC CCTCCCCCTG GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG 4200
GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC 4260
CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG GAGTTGGACC CCCTAGAACC TTGGGCCCAC 4320
CTGTCCCAGT GGCTGCTGGG AGTCTAATTC TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA 4380
GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC CAAAGATGGA TACAAATAAT TTATTTTAAA 4440
AGGTACAATT CACAAGGTTG GAGGGGTAGC TGGAAGTTTC TGTGGTTACC TTGCACTGGG 4500
GGGCTGCCCT GCCTCCACTC TCTCCCCACA GTCCGAGGGC AAGATGAGCA CCCCCACCCA 4560
ATGGCAGGAC CAGCCCTGCG GGGAAATGTC AGCATGAGTG GAAGCACGGC AAGGCCCCTT 4620
CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC AGTTCACAGG GTGTGTGGGT GGGGGGGATG 4680