EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-00188 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr1:9340470-9342940 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs916379chr19341128hg19
rs677665chr19341786hg19
TF binding sites/motifs
Number: 28             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr1:9340484-9340495GCCCCGCCCCC+6.02
KLF5MA0599.1chr1:9340484-9340494GCCCCGCCCC+6.02
RESTMA0138.2chr1:9341495-9341516GGCACTGTGCCTGGTGCTGGG-6.31
SNAI2MA0745.2chr1:9341181-9341191TGCACCTGTT-6.02
ZNF263MA0528.1chr1:9342505-9342526CCCTCCTTTTCCTCCTCCTCC-10.05
ZNF263MA0528.1chr1:9342541-9342562TCCTCTTCCTCCCCCTCCTCC-10.45
ZNF263MA0528.1chr1:9342567-9342588TCCTCCTCCCCCTCCTCCTTC-11.07
ZNF263MA0528.1chr1:9342558-9342579CTCCTTGTCTCCTCCTCCCCC-6.05
ZNF263MA0528.1chr1:9342582-9342603TCCTTCCCCCTCCCCTCCTTG-6.14
ZNF263MA0528.1chr1:9341728-9341749GGAGCAGAAAGATGAGGAAAG+6.18
ZNF263MA0528.1chr1:9342588-9342609CCCCTCCCCTCCTTGTCCTCC-6.54
ZNF263MA0528.1chr1:9342577-9342598CCTCCTCCTTCCCCCTCCCCT-6.71
ZNF263MA0528.1chr1:9342517-9342538TCCTCCTCCTCTCCCTCTTTT-6.75
ZNF263MA0528.1chr1:9342571-9342592CCTCCCCCTCCTCCTTCCCCC-6.82
ZNF263MA0528.1chr1:9342511-9342532TTTTCCTCCTCCTCCTCTCCC-6.92
ZNF263MA0528.1chr1:9342538-9342559TCCTCCTCTTCCTCCCCCTCC-6.98
ZNF263MA0528.1chr1:9342529-9342550CCCTCTTTTTCCTCCTCTTCC-6.99
ZNF263MA0528.1chr1:9342523-9342544TCCTCTCCCTCTTTTTCCTCC-7.16
ZNF263MA0528.1chr1:9342594-9342615CCCTCCTTGTCCTCCTCCTCT-7.5
ZNF263MA0528.1chr1:9342544-9342565TCTTCCTCCCCCTCCTCCTTG-7.63
ZNF263MA0528.1chr1:9342532-9342553TCTTTTTCCTCCTCTTCCTCC-7.76
ZNF263MA0528.1chr1:9342526-9342547TCTCCCTCTTTTTCCTCCTCT-7.83
ZNF263MA0528.1chr1:9342502-9342523GCTCCCTCCTTTTCCTCCTCC-7.98
ZNF263MA0528.1chr1:9342570-9342591TCCTCCCCCTCCTCCTTCCCC-7.98
ZNF263MA0528.1chr1:9342591-9342612CTCCCCTCCTTGTCCTCCTCC-8.22
ZNF263MA0528.1chr1:9342508-9342529TCCTTTTCCTCCTCCTCCTCT-8.4
ZNF263MA0528.1chr1:9342564-9342585GTCTCCTCCTCCCCCTCCTCC-8.7
ZNF263MA0528.1chr1:9342535-9342556TTTTCCTCCTCTTCCTCCCCC-8.87
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_23490chr1:9337921-9342330Colon_Crypt_1
SE_23818chr1:9337980-9341807Colon_Crypt_2
SE_23818chr1:9341834-9342316Colon_Crypt_2
SE_24876chr1:9337785-9342445Colon_Crypt_3
SE_45049chr1:9340486-9342190NHLF
SE_50208chr1:9338047-9342398Sigmoid_Colon
SE_65576chr1:9340212-9341781Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr193404889341044
chr193410909342382
Number: 1             
IDChromosomeStartEnd
GH01I009278chr193384619342291
Enhancer Sequence
CGCCCCCACT CCCCGCCCCG CCCCCACTCC CCGCCCCGCC GCTGGCAGCG GGCAAGGACC 60
CACGACTCAT CCCATGGCCT CCCTCTGGGT AAGTGCTTGT CGACTGAGTC AACGACTGAA 120
TCAGCCGCGG TTGTCAGGGC TCAGCTGGAC TGAGCGCTGC TGCCTGTGGG CGTTTCCTCC 180
TCATGTGTTT TTTATCAGCA GCAGCGGCTG CAGGGTCCCC GTGCTCAGGG GTTGCCTCTG 240
TCGTGCTCAC TCTGCCCCGC GCTCTGTCCA CACCCCTGCT CCATCCAACT CGCAGATGGA 300
GCGGTTTCCT TTGAGCCCCA GTCCTGTCCA AACACACATG GGTGCTGGGC TTTCCCTGTG 360
GCACATTTTC TACCCTCTGT AGGCAGGAAA GAGCAAGCAC ATGGAGGCAG CCCTGTTGTC 420
CTTGGCCTTT CCAGGACACC TGGGAGGAGA CAGCACCCTG TGAGGCTAAG AGCTGGACTC 480
TGGAGTCAGA AAGGTCTGAG TTCAAATCCC ACCCCTGCTG CTGAGAGAGT GGCACAGGGC 540
AGTTTCACCA CTGTGAGCTT GTTCCTCCTC TGTGAACTGA ATAATAAACC CTGCTTTCCA 600
GAAAAGAGGC GCACAGAGAG GACTTTATCA TAGGGCCCAC GATGAGCTCC CGGGGTCCGA 660
GCGAGAGACC CGCAGCACCA CTTGGTGGGG GCAGGGCCGT GTGTCTGCAT GTGCACCTGT 720
TCATCTGCCC ACCGCAGGCT CTCACATACC AGGGCTTTGT CTTCTGCAAG GATGACCAAG 780
ACATGGCCCT GCACTCAGGA AATGACAGGC AAGGAGCGTT CTCAGGGGTG GCAGATGTAG 840
CGAGAGCACT TGGGTCGGAG CCACAGGGCT CTGGGCAGAG ACTGCGGTTC CGTGTTGGGG 900
GAAGGAGGTT AGGGAGTCAG GAAAGATCTC CATCATGTGG GGGCCTTGAA TTAGAAGTTC 960
AGCAAGTGCC ACAGACTGAT TTCACATCCC ACCACAAGTA TTTATTGAGC ACCTATTGTG 1020
TAATAGGCAC TGTGCCTGGT GCTGGGATAC ACGGGGTGGT AGCACAAAGG AAGACACTGC 1080
CCAGGGCTCC TGGCCTGGCG GGGACACAGA CAAGGGCCCA AGGGATGGCA GCCCCAAGGG 1140
GCAGGGCCAA GCTGGGCCAT GCGGAGGGTG CCGTGGGACT GCCTGGCAGG AGCATCTGTC 1200
CACCCTGGGG ATCAGTGCAG AACGTGATTC CATCCTGATG GAAAAGACGT TTCGGCTGGG 1260
AGCAGAAAGA TGAGGAAAGC GCTGCTGTGT GGCATGGGGC CAGCTGCTTC CCCTCCCTGA 1320
GCCTCGGTCT CCTCACCCAC AAGCGGAGGG ACTTGGAGCT CTGCTCTCTC AGGTTCTGGT 1380
GGCTCTGATG GGATGTGACA CCCATGACAT TCCCAGGAGC TGAGAGGATC TCCTGCTACT 1440
TGATAACCTG GAAGGCCCGT GAAAGCTTAG GGCTCTGTCA ATGTAGGAAT CAAGGCTGTG 1500
GAGGCAGATT AGCAGCAGTC CAGCCCCGAG CTGGGACCTG CTCAGCACGC CTCCTCTGCA 1560
CTGGCATTGC CTGCATGTCC AGGTCCTGCC ACAACTGCAC ACTCCACCTC CCAGCTCGAG 1620
CCCCGGGGCC CTCTGAGAGG AGGCAGAGCT TCTCTCTTGG TCTTTGCTGC AGCTCTGCAC 1680
CCTCCCCAGC CGGCCCAGGA GCCAGATGGG ACCCGGCCGA GCTGCAGAAC ACCGTGCACC 1740
TTCCTGCAGT CCTCAGCCTG GGACCTGAGG AGCACAGGCT GATGGCCTGA TGCGGCTTCC 1800
AGACAGAGCT CAGCCCACTC TTGGGAGGTG CCAGCTGCCT GGGTGGTCTG GTATCGGAAT 1860
GAAATCCAGA GGCCAGAAGG AGCCCAGGGT TCAAATTGCC ACCAATTTCC TGAAAGTTCC 1920
TCTAGAGCTC CGGGCAAACC CACCAGTTGA TTGCGGAAAA TAACAGACCC CTCACTTAAA 1980
ACCAGATGTC AGCATCTGTC TTGAACCAGC CCAGGGAGAG ACAGAGGCCC CTGCTCCCTC 2040
CTTTTCCTCC TCCTCCTCTC CCTCTTTTTC CTCCTCTTCC TCCCCCTCCT CCTTGTCTCC 2100
TCCTCCCCCT CCTCCTTCCC CCTCCCCTCC TTGTCCTCCT CCTCTCCCCC TTCCAACTCT 2160
GCAACCAGGT CAACCACAAC CTCTGGCCAC ACAACAGACC CTCTGCAAAG GAAACAACTT 2220
AGCTGGCACC TAAAAATATT GACTTGTGTT TTTCTTTAAA TAGAAAGGAA ACTCAGCTCA 2280
CTCCACCCCA GTGCTCCTCT TTCTGGATTC GAGTGGGCAC CCTGGGACCT CACCCAGACT 2340
CAGCCGCCCC CTCACTGAGC CACCTCGGTT TGGAGGGATG GAGCCATTCA GGATGGAGGA 2400
GGGAGTGGGG CTTGCCTGCT CCTGAGAAAG GTCTCCTGGG GCAGGGTGGG AGTGGGGCTG 2460
ACTAGATATC 2470