EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-03971 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr1:207080250-207082800 
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr1:207081901-207081912CTGCAGCTGTT-6.02
RREB1MA0073.1chr1:207080427-207080447GGGGTGGGGGGGTGGGGGGG-6.06
RREB1MA0073.1chr1:207080435-207080455GGGGTGGGGGGGTGGGGGGG-6.06
RREB1MA0073.1chr1:207080426-207080446GGGGGTGGGGGGGTGGGGGG-6.14
RREB1MA0073.1chr1:207080434-207080454GGGGGTGGGGGGGTGGGGGG-6.14
RREB1MA0073.1chr1:207080432-207080452GGGGGGGTGGGGGGGTGGGG-6.16
RREB1MA0073.1chr1:207080448-207080468GGGGGGGGGGTGGGGGCGGG-6.38
RREB1MA0073.1chr1:207080443-207080463GGGGTGGGGGGGGGGTGGGG-6.57
RREB1MA0073.1chr1:207080454-207080474GGGGTGGGGGCGGGGTGGGG-6.57
RREB1MA0073.1chr1:207080429-207080449GGTGGGGGGGTGGGGGGGTG-6.72
RREB1MA0073.1chr1:207080425-207080445GGGGGGTGGGGGGGTGGGGG-6.95
RREB1MA0073.1chr1:207080433-207080453GGGGGGTGGGGGGGTGGGGG-6.95
RREB1MA0073.1chr1:207080444-207080464GGGTGGGGGGGGGGTGGGGG-7.06
RREB1MA0073.1chr1:207080437-207080457GGTGGGGGGGTGGGGGGGGG-8
Tcf12MA0521.1chr1:207081901-207081912CTGCAGCTGTT-6.62
ZNF263MA0528.1chr1:207081429-207081450GGAGGAGAAGTGGAAGGAGAA+7.34
ZNF740MA0753.2chr1:207080446-207080459GTGGGGGGGGGGT-6.32
ZNF740MA0753.2chr1:207080448-207080461GGGGGGGGGGTGG-6.44
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_10206chr1:207081958-207084707CD19_Primary
SE_10930chr1:207072090-207107411CD20
SE_16055chr1:207079154-207081206CD4_Naive_Primary_7pool
SE_16055chr1:207081985-207083773CD4_Naive_Primary_7pool
SE_17565chr1:207075981-207099113CD4p_CD25-_CD45RAp_Naive
SE_18510chr1:207071597-207081267CD4p_CD25-_Il17-_PMAstim_Th
SE_18510chr1:207081365-207099277CD4p_CD25-_Il17-_PMAstim_Th
SE_22043chr1:207078461-207080572CD8_Naive_8pool
SE_22043chr1:207081717-207084611CD8_Naive_8pool
SE_22585chr1:207078047-207081089CD8_primiary
SE_22585chr1:207081983-207082904CD8_primiary
SE_25533chr1:207077682-207080974DND41
SE_34922chr1:207081822-207084118HeLa
SE_54379chr1:207082325-207083986Spleen
SE_59006chr1:207077980-207107211Ly3
SE_61245chr1:207078603-207107351HBL1
SE_61484chr1:207078352-207107363Toledo
SE_62300chr1:207078312-207107022Tonsil
SE_64397chr1:207077786-207080571NHEK
SE_64397chr1:207081638-207084650NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1207080581207080824
Number: 1             
IDChromosomeStartEnd
GH01I206904chr1207077772207081030
Enhancer Sequence
GCACATATTT TCGAAGCAAG CTGCTGCTGC TTCCCTCTTT AGTAAAGTAC AAAATATATC 60
AAAATTCCTT TCAATGAGTA CTTACTGAAT GCCTACTATG TTCAGACTGC TGAACACTGC 120
CACGCGGGTG TGAACCTTCT CTAGCGGGGG TGGGGAAGGG CAAGCCGGAG AAGCCGGGGG 180
GTGGGGGGGT GGGGGGGTGG GGGGGGGGTG GGGGCGGGGT GGGGACTGCG CAGAACTGCC 240
TCTTGTTGCT GGGTACCACT CTCTTCTTTG TAGCCAGGCC CACGATTGAC CAGCTGGGGA 300
TTAAATTTCT CAGCCTGCCT TGAAGGGAGG TTCACTACAT GGTTAAGTTT CAGCCTCTAG 360
GATGCAAGTG GAAATGGTGG GAAACGTCAG GGTCATGGGC TTAAGAAGCA GCATTCTCTT 420
CCTCCCTCCT GTAAGCTGGG ACGTGCACAC GGTCCTGGTG CCTGTGTACT GACCATGGAG 480
CTGGCAAGAC TCCAGAGGAT GGCGCAGCAA CCAGACAGAG GGAATTTCAG TCCCGAGATG 540
ACCTCTTGGC TCACTGGCTC AGGCCACCTC TTCCTGTCCC TGTCTGAGCC TTTATTTGGG 600
GAGGGGGAAG TAGGCTTCCA CCGTGTGGGC CCTGTCTTTT GGAGTCTGCT GCATTAGCTT 660
AGTCTACATG CGAATTAAAC AAGGGATTTT CTTTTCCCAG GCGGCTGCCG AAGATGGCGG 720
GGGTGCAGGT CCTGGTGCTT GATGGTGGAG GCCATCTCCT GGGCCCCCTG GCGGCCATCG 780
TGGCTAACTA GGTACTGCTG GGCTGGAAGG TGGTTGTCGT ACGCTGGGAG GGCATCAACA 840
TTTCTGGCAA TTTCTACAGA AACAAGTTGA AGTACCTGGC TTTCCCCCGC AAGCGGATGA 900
ACACCAACCC TTCCCGAGGT CCCTACCACT TCCCGGCCCC CAGCCGCATC TTGTGGCACA 960
AGTACGAGGC TTGCTGCCCC AAGAGACCAA GTGAGGCCAG GCCGCCCTGG ACCACCTCAA 1020
GGTGTTTGAC GGCATCCTAC TGCCCTACGA CAAGAAAAAG CGGATGGTGG TTCCTGCTGC 1080
CCTCAAGGTC GTGCGTCTGA AGCTTACAAG AAAGTTTGCC TATCTGGAGC GCCTGGCTCA 1140
CGATGGTGGC TGGAAGTACC AGGCAGTGAT AACCACCCTG GAGGAGAAGT GGAAGGAGAA 1200
GGCCAAGTTC CACTACAGGA AGAAGAAACA GCTCATGAGG CTACGGAAAC GGGCCGAGAA 1260
GAACGTGGAG AAGAAAACTG ACAAATACAC AGAGGTCCTC AAGACCCACG GGCTCCTGGT 1320
CTGAGCCCAA TAAAGACTGT TAATTCCTCA TGCTTGGCCT GGCCTGCCCT TCCTCCATCG 1380
TCGCCCTGGA ATGTGCGGGA CCCAGGGGCA GCAGCAGTCC GGGTGCCACA GGCAGCCTGG 1440
GACATAGGAA GCTGGGAGCA AGGAAAGGGT CTTAGTCACT GCTTTCTGAG GTTACTTGAA 1500
AGCACTCAGG GAATTGTGCA GGTGTAATTT ATCTATGACC AATAGGAAGA GCAACCAGTT 1560
ACTATTAGCA AAAAGGAGTC GGAAGACTAA TTGGAGGGGC CCTACCTTGT GAGTGGGGCG 1620
TCTGTTTAAC TTTCCACCTG GTAATATAGC TCTGCAGCTG TTAGAATGTG CAAGCGCTTG 1680
GGGACAACAT GAGCTTGCTG TTGTACAAAG GGTATTTATA GAACCATAGA CTGGGAAGAT 1740
GTGCGACCAA GGGGTTACAG GAATTGCCTG TGCTCCTCAC CTGTATTTTG TAATCAGGAT 1800
CAAATAAATT ATTTTTAAAG AAAAAAAAAA CAGGGATTTT TACCACACCC TTTTAAAAAA 1860
AGCTTTATTC TGGGCTCTGC GTGTTTTGGA CACTGTAGGC TGCTTTAGAG AATAAAAAGC 1920
TTTCTCATCT CAATTCTTAA AGATGAACGG ATAAAGGCTT TCTACCCAAC CATCAGTGGC 1980
CCTGAGTGGA AACGCGAGTT CCCTCCATCC ACTCTAGATT TAAAGATGAA TCCTCCTCAC 2040
TCAAGGTGTT GAACCCTGTC TACATCTCTC CCAAGTCATC CTCTAGCCAA GCTTAACCGC 2100
CTCCAGAGAA AGGTAAATTA CCTCCTCTCA TCTTCGAGAG TTTACTAGAA AGTTCTCGCG 2160
CACAGGAAGG TGAACTGTCT AGGTAGCTTC CACCTCCCTA GGACCCCCTA GAAATCTAAT 2220
CTCCTCCACG AGAAAGCCTT TCACATAACT GTGGAGCTGC CACCTATCAT TCTCTGCTAA 2280
GCCAGCTGCA TCCAGCACGC AGGTATCCCG TGACAACTGC TTGGCTAGAA GCCACGGAAC 2340
CAGGTCTTCT ACAGTTCCCG GTATTCAACC TCCTGACACC AAACAAGGAG GAAACTAAAA 2400
CAACTTGTTC CTCGGCTCAG GGCCCAGGAG CTGCTGGGAA ACCCGCTCTC CGGATCGCGG 2460
CGGCGGCGGC GCGGGAAGCC ACACTCGGGT CCCCGCCCAG GGCTGGGGCC GCCCAGTCGG 2520
GCCGCGGCTG CCAATCAGGG CAGGAGCGGA 2550