EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS098-30695 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr2:85152560-85154500 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr2:85153002-85153021GGGTGCCTTCTGGTGGCCA-7.09
CTCFMA0139.1chr2:85154305-85154324GGGCGCCATCTGGTGGTCA-8.12
CTCFMA0139.1chr2:85153109-85153128GGGCCACCAGGGGGCGCCA+8.48
Foxd3MA0041.1chr2:85153523-85153535GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr2:85153527-85153539GTTTGTTTGTTT+6.32
KLF14MA0740.1chr2:85153318-85153332GGAGGGGCGTGGCA-6.06
SP3MA0746.2chr2:85153319-85153332GAGGGGCGTGGCA-6.08
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_10467chr2:85152411-85153224CD19_Primary
SE_10467chr2:85153647-85154542CD19_Primary
SE_14858chr2:85152185-85154666CD4_Memory_Primary_7pool
SE_15828chr2:85152431-85154332CD4_Naive_Primary_7pool
SE_17329chr2:85150774-85154544CD4p_CD25-_CD45RAp_Naive
SE_18307chr2:85150779-85154763CD4p_CD25-_Il17-_PMAstim_Th
SE_19290chr2:85152241-85154577CD4p_CD25-_Il17p_PMAstim_Th17
SE_22056chr2:85152158-85154691CD8_Naive_8pool
SE_24195chr2:85153080-85153423Colon_Crypt_2
SE_24195chr2:85153770-85154270Colon_Crypt_2
SE_25084chr2:85152974-85153457Colon_Crypt_3
SE_25084chr2:85153774-85154325Colon_Crypt_3
SE_27502chr2:85152280-85153403Esophagus
SE_27502chr2:85153883-85154364Esophagus
SE_32545chr2:85152205-85153149GM12878
SE_32545chr2:85153223-85155068GM12878
SE_34685chr2:85152236-85155103HeLa
SE_35873chr2:85151006-85155048HMEC
SE_43289chr2:85152136-85153652Lung
SE_45342chr2:85153616-85154158NHLF
SE_47378chr2:85152158-85155396Panc1
SE_50337chr2:85152152-85154468Sigmoid_Colon
SE_52528chr2:85152250-85153473Small_Intestine
SE_52528chr2:85153680-85154430Small_Intestine
SE_54030chr2:85152520-85153581Spleen
SE_54030chr2:85153652-85154458Spleen
SE_55909chr2:85152237-85153558u87
SE_55909chr2:85153733-85154923u87
SE_57573chr2:85153731-85154373VACO_503
SE_58212chr2:85152446-85152965VACO_9m
SE_58212chr2:85153042-85153511VACO_9m
SE_58212chr2:85153624-85154273VACO_9m
SE_59563chr2:85151112-85174538Ly3
SE_65145chr2:85151065-85153445NHEK
SE_65145chr2:85153665-85154405NHEK
SE_67823chr2:85152237-85153558u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr28515400085154377
chr28515304685153400
Number: 1             
IDChromosomeStartEnd
GH02I084923chr28515092685154924
Enhancer Sequence
AGCCGAGGGA GCCTTCCAGA GCCTCTAAGT CACCTCTCTA GGAGGCTGTC TGCCTGGCCC 60
ACACACAGGC AGGCCCCATT CTTGGCCTCC CCAAGCCAAG AGGGCACAGA CTGATGATCC 120
AGGGCAGGTC TAGGCAAGTG GGGCATGCAG GGATGTTGTA TTAAAGCTTA AGCATCATGA 180
GAGGATCTGA TGACTCAGGG AGCAATTTCT TGAGCCCATA TTGTCCACCT GGGAAGAAAT 240
TGTGGCTGAG GAGTATTCAG GAGCAGCTAT GGGGGAGAGA GGGGCAGAAA TACACCTCAA 300
GGTAGGCCTC TACTGGGTTC AGGAGGTCCC GGGGCTAGGC AGAGAAAGGC AAGCTTGAGA 360
CCCAACAGCG CCACCCACCA TGCATAAATC GGTTCCCTAG TCATCAATTC GCTTATGAAT 420
ACGGAGGCCC CGGAAAGGTG AAGGGTGCCT TCTGGTGGCC AGCTGTGGAG GTGGCCTCGG 480
AGAAGGGTGA CCCGAGTGAC AAGTTGCAGT GAGCGCTGGC TGCGTGCCCA GCCGCGTTGC 540
ACAACTCCCG GGCCACCAGG GGGCGCCATT CTCACACATT CCAGAGCAAA CGGTGCTCCT 600
TGGAGTTGAG CGGCGCGACG GTCCTGCAGC AGCTAGCCTG GGATGTACCC ACAGCTCACC 660
GGGGAGTCCG GGCCACACGT CAGCTGGATC TTGAATGAGA TGAAGACGGG GAGAAAGGGC 720
CTTCCGGACA AAGGGCTTAC GCCCTGGATA AAGGGCGTGG AGGGGCGTGG CACGTTCAGT 780
CTGGACACAG CATAAAGTGC ATTGGAGAGA GGCGGGAGAC AGGATGGAAA GGAGGGTGGG 840
AAGAGCTATG AAGCTCCCCA GGGCCTTGCT AACGCGTTTG GACTTTATCC CGCGCCAGAC 900
TTTTTAAAGG TGGTAAGTAG TTTACAGATG TGCGTTTTGA GGCCAGCACA TTTTGTTGTT 960
GTCGTTTGTT TGTTTGTTTT TCTTTGAGAC GGGGTCTCAC TCCCAGGCTG GAGTGCAATA 1020
ACGTGATCTC AGCTCACTGC AACCTCCGCC TCCCAGGTTC AAGCGATTCC CCTGCCTCAA 1080
CCTGTCGAAT AGCTGGGGCT ACAGGCGCCC ACCACCACGC CTGGCTAATT TTTGTATTTT 1140
TAGTGGAGAC GGGGTTTCAC CACGTTGGCC AGGCTGGTCT CGAACTCCTG ACTTCAGGTG 1200
ATCCTCCCGC CAAGGCCTCC CAAAATCCTG GGATTACGGC CATCGTGCCG GGCCAGCAGC 1260
ACAGCGTCTT AAGCAATTTT GGATATGAAT ACCTTCGAGA CGAGCTTGCG CTCCCACAGA 1320
CCCCACCACT CCTACAGTCT GTAATTACCC CCAGCTGCAC CCATATGCGT AGCTTCCCTG 1380
GTCCAGAGGG ACGTGCGTGT GTGACCCTGC AGGATAGTGG GGTGGCCCTG CATGGCATGG 1440
CTGCCAGTGC TAAGAGGGGT GTGCCGCCAG CCTCTGATCC CTCTCACCGG CGGGCCCCCC 1500
ATCATCATCA CTATATGATG ACCTGAGGCG TCCAGGCTCC CGAGGAAAGC CTGCCGCCCT 1560
GGTTCCTACA AGGGACGCCT AAACACAGAG TCCTAAACAC AGAGTCCTAA ACACATGCAG 1620
GGTTGGAGGG AGACTGACGA ACTCAACTAC CAGCCTGCAG TCGGCAGCCA TCAGCGGATT 1680
GCAGGTACCC CGCGTGCGTG TCTCGGCTAC AGTGCGGAAG ACAAGAGGCC TTAGGAAGTG 1740
GGAACGGGCG CCATCTGGTG GTCATCTCTG GAGTGACAGC AGAGAACTGG AACATATTTT 1800
ATATTTTGTT TCCACTGCTC CATGACTTGA CTAAAGCAGA AACAATTCGG AGAGTACTGT 1860
AGTATTAAAT ACCTAAGGGC CACACCAGGC CAGAAAGCAA CAAAAAAGAA ATGCTAAAAA 1920
GAAGTTCTTC AGAGAGGGAT 1940