EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-00020 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr1:1001960-1006630 
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
CAGCAGGAAT GCCGGTTCCT GTACCCTCGG AAGGAGGGGC AGAGTGTGGA GAACAAGCCC 60
AAGAATCACT ACAAGAACAT CCTTCCCTGT GAGGGCGGAG GCCAGGGCGT CACCCGTCGG 120
GCCTGGGGGA GGTGGGGGGC AGGCCGAGCA TCTGCCACCG CTGACCTGAG GCTCCCCCTT 180
GCATACCCTG GACCCTCCAT CTCTGCTCAC CACAGGGTCT GCGGGCAAAG AGGCAGGGTG 240
AGGCCCACGA GCTGTGCCCT GGAGAACTGA GCGGCACCTC CCTTCCCAGT TGATGCTACC 300
CTTGAGTCAT CCTGCTCAAC GAGGATGACA GCGGGCCCGG AGCCGACTAC ATCAGGGTGG 360
GTGTGTGCGG GAGGCGGGGC CTGGGCCCAT TGCTCCTGGG GGGCTCAGGA AGAACCAGGG 420
TCCCCAAGGG AGGGGTGGGC GGCAGTCTCC AAGGGGTCCT CAGAGAGGCT GGACGGGCAT 480
TGGTCCTCAG CCCCTTGCTG GCCTGGAGTG AGGAGTGTGT TTAAGCCACC AGGGCTCTTT 540
GCATAATATT TGTGTGTCGT TTGCATATCA TTTGCATAGC ATTTGCATGG ACTTGTTTGT 600
CCTCTGTTAA CAGCAGCAGT TGGCCTCATT CCCTTTCAGA CTGACCCTGA GGAGGAGCCG 660
GGCCATGGCA GGGGCAGGGT GGACATCCCT TGTGGCCCTG CCCCGCCGCA CCTGCACCTG 720
CACAGCCCGC GTGGGCCCGC CCCGCCGCAG CTGAAGTGCA CCACCATGGG CCCGGCCCGC 780
GGCTCGCGGC TCGCGGCTCT GGGCCCGGTT CACCTCGTCC CGGAAGCCGA GGACGCCGGC 840
GGGATCGGTC CGGACGCCGT AGTCCGGCCA GCCGAAGTAC TGGAAGTGCT GCACCGTACG 900
CTGTGGCTCC TCCCCGCGGG GCAGGGCCTC GCGGGCGCAG GGTGTACATC GCCTGCAGGG 960
CTGTCTGCAG GCCTGTCTGC AGGCCACGGT GGCTGCTTTC TGGGCCACGG TGCACCAGGA 1020
GAACACGCGT GTCATCGTCA TGACCACCAG GGAGATGGAG CGGGGCCGGG TAGGGGTGCG 1080
GTGCCAGTGC TCCCAGTGCC CATCCCACCC CGTGCATCTT CGGCTGCCCA AGGCCCTTCC 1140
CGACCAGGCC AAGGAGGCTG TGGGACGCCG TGGGAGTGGG GAGGCTCCCA CAGAGCCCCG 1200
TGGCTGCACG TACACACCTG CGTCTCTGCA GGTCGCAGGG GCGGGGTGCC GAGGTGCTGC 1260
CAGCAAGGCT GATGCAAAGC GCTCCCCTCG GAACAAGTGT TTCCGGGACT GGCCAGAGCT 1320
GCCCGGCAGC CAAGAGTTCG GCCGTGTGCA CATGCGCGTC CTCGGCAAGG GCCAGGCCCA 1380
GGGCTACTGC GTGCGGGAGC TGCAGGTGTG GCGGCCGGGC CAGGTGAGCC TGGCGGCTGT 1440
GGAGCGTGCC TGCTGTCGGC CTGCACTGGG AGACCCCACA CCTGCCTGCA TCCAACCCCA 1500
CTGCCTTTGG GGGCTTCCAC ACCCCTCAAC CCAGGAGGTG CATTCCAAGC CTGGACAGGG 1560
GTCACTGACG TGGCCACATT CTCAGCCCTG GGCTGGCGGC CGCTCCTCCC ACACACCTCT 1620
CCAACTGCAG CTTTGGTCTC CGTTGTATAC CAGAGACGCC CATTTCTGCT CCGGGCAGAT 1680
TACCTCGTGT TCCCTCCAGC CCCCGCCCAG TGTGTGTGGG GGGGTCCTCC AGGACCCCAT 1740
GGACCCCTCA CATTTGGTTT TTCCTTATAA AATAACTGTC CTCACAGCCT GCTTCGCCCG 1800
CCCCCAGCTC CCTCTTCCCT TCCCCAGGCA CCTGAGCCAC CTGGGGCCAT CTCGGCGCCC 1860
CCTCCCCATT TCCTTCCTCC TCCTCCTGCT CGCCTTGGCT CCCGCAGCCC CTCCGCTTGG 1920
GCACTCCCGG AAACCCAGCT GTGCCTCAGC CTCCTCCTCC CACCCTGGGG TCACACTCAC 1980
CGCTTGCCCC GCTCAGGAGG AGCCACAGCG TACGGTGCAG CACTTCCAGT ACTTCGGCTG 2040
GCCGGACTAC GGCGTCCGGG CCGATCCCGC CGGCGTCCTC GGCTTCCGGG ACGAGGTGAA 2100
CCGGGCCCAG AGCAGCAAGC CGCGGGCCGG GCCCATGGTG GTGCACTTCA GCTGCGGCGG 2160
GGCGGGCCCA CGCGGGCTGT GCAGATGCAG GTGCGGCGGG GCGGGGCCAC GCGGGCTGTG 2220
CAGGTGCAGG TGCGGCGGGG CGGGGCCACG CGGGACGACG AGGGCGGAGC CATCGGGTGG 2280
GCGGGGGCGC CCCCGCCCCC GCCCCCCACT CTCGTCAAAG GCCGCCTAGT TTGTCCTCAG 2340
TGGGGGCATC GGATGCACGG GCACCATCAT CGTGATTGAC ATCCTGGTGG ACGTCATCCG 2400
CAGGCAGGGC GAGCCGCTCC ACTCTGGGTC CCCCCGCCCT GCCCTGCTAT AGCCCCACCC 2460
CTCCGGGCGA CCCCACCCCT CCGGACGACC CCACCCCTCA GGACGACCCC ACCCCTCAGG 2520
ACGACCCCAC CGCTACCGGC AAGCCCCGCC CCTCATCAGC AGCCCCGCCC CTGCCTGCCG 2580
GCACCTTCCC CCCATCCGTA GCCCCTCCCC AAGCGCGCTT GTCCGCAGGG CTGGACTGCG 2640
ACACCGACGT CCCGAAGACG ATCCAGCTGG TTTGGCGGCA GCACTGGGGA ATGGTGCAGA 2700
CGGAGGCTCC GTACAAGTTC ACGTACCTGG CGCTGCAGCG GCACATCCGG GGCGAGTAAC 2760
TGCGCCTGCG CGAGCAGGTG GGGGCGTGGC CCTGCGGGGC GTGGCCTGTG CGGGCGTCGC 2820
CATGGTGACC GGCGGCCCCT CCCCCCAGCG CGAGCCGCCT CAGGAGCGCG AGAACCAAAA 2880
CGTGGGCGCC GCCCCCCGCT AATCGGGTTG CAGCCCCCGG CTCCCCGGGC ATCCCCGGTG 2940
TGAGTGGAGC GCCGGGGCCG GTCCGGAGTC CTCTGGGAGG GACTGGGACG TGCGGGGTGC 3000
AGGGCTGAGC CGCTGCTCCG CGCGCAGAAC CCCGCAGCCC TGGGACGGCG AGGACGCGAA 3060
CCTGCGGAGC CGCGGGTGTC TGAGGAGCCG CAGGGAACCC CCGGCCTAGC CGCGCCCGCG 3120
TGTGGCCGGA GCTGCGGGCC GGGACTGTGT CCAGGACAGA GCCACAAGCT TGTCCCCAGC 3180
TCAGGGAGGT CCAGGGGCGG CAGAGGGAGC GACAGGCTGC GAAGCCCACC GGTGACCACG 3240
TGTGAACCCG CGTGCGCCCC CAGCTCGGCC ACTCCGTGCG GGTCTGCCCT CACCGCAGCT 3300
CCGGCCTGCC GGCCCTGCCT GCTCCCGTGG TCTGGGATGT GGCCCCGGTG AGGACCCGGC 3360
CCCATCAGGC ACAGGGTGGA TGTCTGTGGA GTGAGGTGTG TGTGACATAT TCATGTGACC 3420
ACCCGTGCAG CGTCACGCGC CTGGCCCTGC CGATGACAAG GGTGTGGGCC TGCGTGGGCA 3480
TGACTGTGTG TGTGACACAG AGTGATGTTG CTGTGACCCG TGGCTGCACT CCCCACATCA 3540
CCGGCTTTCA CAGCCTTCCG GTAAAGTGCT GTGTTCTCCC TTCTGTGTCT TCGCTGGGAC 3600
CTGGGGCAAG GGTGGGTGTG GCCCCCACAG CTGGAGTCAG CTTCTGTGGG GCCTTCCCGA 3660
GCCCTCCCCA CCCTGGACCA GAGGCCCAGC TGGTTGGAGC AGGAAGTACC TGGGCTCTGG 3720
GGTCAGGGAT GGGAAGGCTG AGGAGGCCTG CGTGAGCTGG ACCTGGCCTG GGCCCTCCTG 3780
GCCGTGCCTG CCTGGTGGTG CAGGATTCCT GGGGCTGATG ACAGACGGGG TAGGGCTGGG 3840
GTTGGCGAGC CTCCTGCCGA TACCTCACGT AGCTGACCTC TGACTCTTCC CCAGCCAGGC 3900
TGGCCCTGGG AGTTGCCGGA GAGTCAGTGG ATCTGCAGGC TGCACGCTGG CTGTTACCTT 3960
TGCTTCTGGG TTCCCACAGG GGTCATGGTT CTGTGGTTCT CCAGTCAGGG ACCCTAGCAG 4020
GGCCATGGGG CGTGACTTCC TGGAGGTGTG GCCTAGTATG GCCACGGCAG AGGATGGGGG 4080
AAGAGAAAGG CCCCCTTTGT CAGCCCCCGG GCTCTGAACC AAGCTGAAGC CCTCCCCCTG 4140
GTCCAGCCTG CCCTGCCCCA AGTGTCCTGG GCCTCTCCCC ATCTCCCTGG GGAGCCTCAC 4200
ATTGCTGAGT CGCCAGCCAA CTCCAGAAAC CCCCAGCCTG TCTGCAGCCA GAGGGGCTGG 4260
GAGTTGGACC CCCTAGAACC TTGGGCCCAC CTGTCCCAGT GGCTGCTGGG AGTCTAATTC 4320
TGTCAGGGTA TCCTCTGGGT TGAGGCTGCA GCAGGGGCAC CCAGGGTGAG GCCCTCTTGC 4380
CAAAGATGGA TACAAATAAT TTATTTTAAA AGGTACAATT CACAAGGTTG GAGGGGTAGC 4440
TGGAAGTTTC TGTGGTTACC TTGCACTGGG GGGCTGCCCT GCCTCCACTC TCTCCCCACA 4500
GTCCGAGGGC AAGATGAGCA CCCCCACCCA ATGGCAGGAC CAGCCCTGCG GGGAAATGTC 4560
AGCATGAGTG GAAGCACGGC AAGGCCCCTT CCTTCTTGGC AAGGGGCTTC CCTGGCAGGC 4620
AGTTCACAGG GTGTGTGGGT GGGGGGGATG CTGACCAGCT GCTCTCCTGG 4670