EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-32268 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr7:102058150-102060900 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12534945chr7102058179hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELF3MA0640.1chr7:102058371-102058384TTACTTCCTGGTA-6.17
ELF5MA0136.2chr7:102058372-102058383TACTTCCTGGT-6.02
EWSR1-FLI1MA0149.1chr7:102058361-102058379CTTGGCTTCCTTACTTCC-6.44
FOXF2MA0030.1chr7:102059173-102059187ATTGTTTACCGTTA-6.46
HES2MA0616.2chr7:102058638-102058648GGCACGTGCC+6.02
HES2MA0616.2chr7:102058638-102058648GGCACGTGCC-6.02
SOX10MA0442.2chr7:102059294-102059305TTCTTTGTTTT-6.62
ZNF263MA0528.1chr7:102059995-102060016TTCCCCTGTTCAGCCTCCTCC-6.32
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_09880chr7:102059742-102062387CD14
SE_10269chr7:102058692-102059339CD19_Primary
SE_10269chr7:102059706-102062816CD19_Primary
SE_11022chr7:102052786-102078230CD20
SE_12084chr7:102058664-102059132CD3
SE_13111chr7:102060512-102062095CD34_Primary_RO01480
SE_13774chr7:102058659-102062610CD34_Primary_RO01536
SE_17654chr7:102055359-102059666CD4p_CD25-_CD45RAp_Naive
SE_17654chr7:102059850-102061984CD4p_CD25-_CD45RAp_Naive
SE_18074chr7:102055362-102059776CD4p_CD25-_CD45ROp_Memory
SE_20233chr7:102055105-102058612CD56
SE_20233chr7:102060406-102062654CD56
SE_22677chr7:102054526-102059670CD8_primiary
SE_31146chr7:102060624-102061839Fetal_Thymus
SE_53584chr7:102059793-102062248Spleen
SE_58603chr7:102040407-102092313Ly1
SE_59253chr7:102055636-102092627Ly3
SE_60339chr7:102055866-102075560Ly4
SE_60478chr7:102022497-102092339DHL6
SE_62031chr7:102047957-102092277Toledo
SE_62443chr7:102048336-102086597Tonsil
SE_66677chr7:102060589-102061733Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7102060396102060446
Number: 2             
IDChromosomeStartEnd
GH07I102419chr7102059694102062500
GH07I102414chr7102055205102059635
Enhancer Sequence
AAACTCCGGG CTCAAACAAT CCTCTCGCCT CAGCTTCCTG AGTAGCTGGG CCCACAGGCA 60
TGCACCACCA TGCCCGGCTC AGTTTTAAAA TTTTTTTGTA GAGACAAGGG TCTCGCTATA 120
TGGCCCAGGC TGGTCTCAAA CTCCTGGGCT CAAGCAGTCC CCCTGCCTCA GCCTCCCAAA 180
AGTGCTGGAA TTACAGGCAT GAACCACCAC ACTTGGCTTC CTTACTTCCT GGTACTATAG 240
GATATTCCAG ACTCGTGTCT TGTGTTTCCT GCCCTGGACC TGGGATCAGC CATTTGTCCA 300
AGAAGTCCTG GCTGCTGCTT TCTTCTTCTT CTTCTTCTTC TTCTTCTTTT TTTTTTTTTT 360
TAAGATAGAG TTTCACTCTT TGTTTGCCCA GGCTGGAGTG CAATGGTGCG ATCTCGGCTC 420
ACTGCAACCT CCGCCTCCCG GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG 480
GGATTATAGG CACGTGCCAC CACACTCAGC TAATTTTTGT ATTTTTAGTA GAGACAGGGT 540
TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTAGCCTC AAACAGTCCA CCTGCCTCGG 600
CCTCCCAAAG TGCTGGGATT ATAGGCGTGA GCCACCATGC CTGGTCCCTG GCTGCTTTTA 660
GAGAAATGGT ATTAAAATGG TATTAAAACC CAAGGTCTGG GGACTAGGCA TGTTCTGTGC 720
TACTGGATGG TTGCTTTTAG GCTCTCTCAG CTGACAGAGC CAGGAAATTT ACCTGTGTAC 780
TCCACCAGTA TATATGTACA TATCTGTCAA TACTAATACC CATAACCATC CCCATCCATA 840
TTACACTAAC ATGAGTTCAT ACTGATGTCT CCAAGTCTAG CCCAGTATGA CATAGCTCAT 900
TCTAGCCTTC TCTCCTTGTT TCTCTGTCAC CTCTCACTCC AATAGTGAGT ATCTTTGCTA 960
CCACCATCCA CTAGCCATTT GCTTAATTGC TCAATGCCAG CATACATGGA TAATGGTTTC 1020
AGAATTGTTT ACCGTTACCC TGGGGGAAGC ACCATTATCA ACTAGAGGAC ATTGCTATGT 1080
GCAGTCCCTT CAGCCTTACA GCTTACAGAG GCCACTCATT TCAAGAATTA CTTAGATCAG 1140
CACTTTCTTT GTTTTTAATG TTTAAAAAAA AAATTTGAGA CGATGTTACA TTTTATCGCC 1200
CAAGCTGGTC TTGAACTCCT GGGCTCAAGC GATCCTCCGG CCTCAACCTC CCAAAGTGCT 1260
GGGATCACAG GCATGAGCCA CCACACCTGG CTGATCAGCA CTTTTCCCCA CACTCCCTTC 1320
ACAGAGGTCA TTTCGTACAT TTATGATACG TTTGGATTCA TGTGTCACCT TCTGCGTTCC 1380
ATCCTGGGAC CCTGACTTCC TAAATGACTT TTAAAATTAG CATAATTCAG CCAGGCACAG 1440
TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCTGAGG TGGGCAGATC ACTTGCGGTC 1500
AGGCGTTCAA GACCAGCCTG GCCAACATGG TGAAACCCCA TCTCTACTAA AAACACAGAA 1560
ATTAGCCAGG CACTGTGGCG GGCACCTGTT ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA 1620
AAATCACTTG AACCCTGGAG GTGGAGGTTG CTGTGAGCCA AGATCACACC ACTGCAGTCC 1680
AGCCTGGGTG ACAGAATGAG ACTCCGTCTA AAAAAAAAAT AGCATAATTA AGTTTTAATT 1740
ATTTGTGCTG TAAGGTTCTG TGGATTTTGT CAAACGCATA GTACCATGTA TCCACCACTG 1800
CCGTATCATA CAGAATAATT CCACTGCCCT AAAACAATTC CGTGTTTCCC CTGTTCAGCC 1860
TCCTCCCAAC CCCCAGCCCC TGGCAGCTGT TTACTGCCTC TGTGGTTCTG CCTTCTCCAC 1920
ACTGTCATAG AGTCGGAATT AAATCGTATA CAGCCTTTCC AGATTGGCTT CTTTTGCTTA 1980
CCAGAACGTG GCTTAATGCC CCATTCCTTT TGCCAAGTAG TTTTCCACCG TCAAGATAGA 2040
CCACCGTTTA CCCACTGAAG GACAGCCTGG TTGTATCCAA GTTTTGGTGA TTATGGATAA 2100
AGCTTCAACA GACATTTGTG TGCTACTGTT TTTTTGTGTT TTTGTGTGTG TGTGTGTGTG 2160
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTTTTTGAG ATGGAGTCTC TCTGTCGCCC 2220
AGGCTGGAGT GCAGTGGCGC AATCTCAGGT CACTGCAACC TCCGCCCCCT GGGTTCACAG 2280
GTTTAAGCAA TTCTCTTGTC TCAGCCTTCA GAGTAGCTAA GCCAGGCATC TGCCACCACG 2340
CCTGGCTAAT TTTTGTATTT TTAGTGGAGA TGGGTTTTCG CCGTGTTGGC CAGGCTGGTC 2400
TCGAACTCGT GACCTCAAGT GATCTGCCCG CCTTGGCCTC CCAAAGTGCT GGGATTACAG 2460
GCATGAGCCA CCGTGCCTGG CCTTGTGTGC TAGTTTTTGT GTGCACATAA GTTTCACATC 2520
AACTGAGTAC ATCTGCAGGA ACATGATTGC TGGGTTGTAT GATAGGATTA ATCTTGTTAA 2580
CTTTGTAAGA AACTGCCAAA CTGTCTTGCA AAGTGGCTAT TCCATGCTGT ACTCCCACCA 2640
GCAACGATAG TTTCTCTTAC CTCACATCCT TCTCAGCACT TGGTATTGTC CGTTTTTTGA 2700
ATTTGAGCCA TCCTAATATA TGTGTTGTGC TTTTTGTTTT GATTTGTGAC 2750