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

TagContent
EnhancerAtlas ID
HS091-01272 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr1:36833920-36835860 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr1:36834767-36834778GGGGGCGGGGC-6.02
KLF5MA0599.1chr1:36834768-36834778GGGGCGGGGC-6.02
MAFGMA0659.1chr1:36835749-36835770GTTTTGCTTAGACAGCATTTG-6.16
MAFKMA0496.2chr1:36835750-36835769TTTTGCTTAGACAGCATTT-6.36
MAFKMA0496.2chr1:36835750-36835769TTTTGCTTAGACAGCATTT+6.44
SP1MA0079.4chr1:36834766-36834781GGGGGGCGGGGCCTC-6.52
SP3MA0746.2chr1:36834766-36834779GGGGGGCGGGGCC-6.11
SP4MA0685.1chr1:36834764-36834781TGGGGGGGCGGGGCCTC-6.48
ZNF740MA0753.2chr1:36834762-36834775GTTGGGGGGGCGG-6.27
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_00264chr1:36830417-36836190Adipose_Nuclei
SE_04744chr1:36834192-36835611Brain_Anterior_Caudate
SE_06364chr1:36834212-36836470Brain_Hippocampus_Middle
SE_08563chr1:36833979-36836143Brain_Inferior_Temporal_Lobe
SE_09252chr1:36830385-36842613CD14
SE_11159chr1:36829411-36836756CD20
SE_13460chr1:36834212-36834720CD34_Primary_RO01536
SE_14627chr1:36834052-36836571CD4_Memory_Primary_7pool
SE_18215chr1:36830641-36835788CD4p_CD25-_CD45ROp_Memory
SE_18903chr1:36830547-36835076CD4p_CD25-_Il17-_PMAstim_Th
SE_24109chr1:36834425-36834766Colon_Crypt_2
SE_26702chr1:36834464-36835879Esophagus
SE_28867chr1:36832956-36835062Fetal_Intestine_Large
SE_31812chr1:36835092-36835735Gastric
SE_34522chr1:36834836-36835921HCT-116
SE_38175chr1:36833999-36834841HUVEC
SE_50223chr1:36834311-36836130Sigmoid_Colon
SE_52539chr1:36834367-36835842Small_Intestine
SE_55982chr1:36834818-36835897u87
SE_60634chr1:36834487-36864245DHL6
SE_62579chr1:36814176-36867515Tonsil
SE_65601chr1:36834744-36835707Pancreatic_islets
SE_67689chr1:36834818-36835897u87
SE_69005chr1:36834440-36836184H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13683433336834787
Number: 1             
IDChromosomeStartEnd
GH01I036365chr13683073736836194
Enhancer Sequence
ACTGGAGTGC AGCTTCCACC TGCCAGGCCC AAGTGATTCT CCCACCTCAG CCTCCTGGGT 60
AGCTGAGACT ACTGGCACAC ATTACCATAC CTGGCTAATT TTTAAAATGT TTTGTAGAGA 120
GGAGGTCTTG CTATGTTGCA TAGGCTGGTC TCGAACTCCT GGGCTAAAGT GATCCTTCCA 180
CCTTGGCCTC CCAAAGTGCT AGGATTACAG GCGTGAGCCA CCACCCCCAA TCTACTCATG 240
CTATTTTTTT TTCCAAAAAT GTATAATTTG AATCTAATCA TGAAACAAAC CCAAATTGAA 300
GGACATTCAC AATAGGCCTG TATGTTTCAA AAACATCCAT GTCAGACAGT TAAAGAAAAG 360
CTGAAGAATG ATTCTAGATT AAAGGAGACT AAAGACATAC AACAAAGAAA TACAATGGGT 420
GATCTGGGAG AAAAAAGGTA TAAAAGACAT GATTGGACAA CTGGTAAAAT CTGAATATAG 480
ACTGTTTATT AGATAATAGT ATTGTATCAG TTAAATTTCC TGAACTTGCA AATTGCATTG 540
TGGTTCTACA GGAGAATGCC CTTGTTCTTA GGTGATACAT ACTCAAGTGT TTTGGGGTGA 600
AGGGTCATGA AGTCTGTAAC TTACTCTCAG GTCCCCCGAG GCAGAGGAGA AAATCCAGCC 660
TGCTCGAATA GCTCCCAAGA CCTGATTCAC AGGTTCAGAG GGACCTGTGG CTTGTGGGTA 720
CACAGCCCAC AGTGGCAGAA CTTGCAGTCT CATATATGTT GGGCAGAGCC AGCCTGGCAT 780
GAACAGGAAT TCAGTCTTTT ATGGCCCCCT CTCTTCAACA CTGTGCTATT ATCAAAGAAT 840
TGGTTGGGGG GGCGGGGCCT CCATGCAATC TCCAGGCCTG CCACCTGGTG GTGTCTTTCT 900
GTAGTGCAGC TTCACAGGGT TTTTCTGCAC CAGGTGCAGG ATGGTGGGGC CCTGCTCTCC 960
TCAGGCTGAT CAGGAAGGAT GCACTCCATG GGAAGAGCTC ACCTCAGCCA CCTGTGTAAG 1020
TGGGGCTGGG CAATCAGATC CCAGGAGGCT GCCGTCTCTC TGCCTGCTGT GGAGGTCCTC 1080
CAAGGGCTCC ATGCTCTTCA GGAAGAACCC CAATTCCTCA GTGAGCCTAA GCAGACCTAG 1140
AATACTTCTC CAGCCTCACT GCCTTTATAT GCACCCTAAA TCCAGCCACA CCAAATGACA 1200
CAATCCCGAG TATGCCATGA ACACCCCTGC CCCGCCCAAC TCTCCCTGGT TGGCACATCC 1260
TTCTCCCTTG GTCCTCACTG AAATGTCACC TGCTGCAGAA AGTCTTCACA GAAGGCCTCC 1320
TGCCAAAGCT GGCTGCTCCT CCTCCAACCC CCAGAGCACC TGAGTACACC TCCGTCCCCT 1380
CCCACTGTGC TGCAACCATT GGTTTATCTG TCTGACTCCC CCATCTCAGG CTGTGGGCTC 1440
CCTTGAGGGA GCAACTCCAA TCCACCGCTG CCTCCCTGCA CCCAGCCCAC TGCCTGGCGC 1500
AAAGCTGGAA GAGAACACAG TGTGGGGCTG TTTGCTGGGC ATCTATAAGG CACCATGGTC 1560
CCTGCTGGGG CAGGAGACAG AGGCAGTTGA ATAAAGAGGT ACAAGGTGTG ATTCACAGGA 1620
AAACTCTGTC CAAGGAGGGG CCAGTGGCTG GAGTGGGACC CTGAAGAAAG TACAGATGGT 1680
CAGACTAGCC AGTATCTGCC AAGTCATGGC TGGAGACAGG GTGCCACAGC TGTAGGTAAC 1740
TGGGGCTGCA CTGGATAGTC TGTCCAGGAA AAGTCCCATG TCAGAAATGC ATGAGGCAGA 1800
ATGGGGACTA GGCTGGCTGA TTACCGGGGG TTTTGCTTAG ACAGCATTTG CTGCTGGAGA 1860
GCAACCCCTA CTGAAGAATT AAAACTGTTC ATAACATGCC TGCAGCTGTG CAGAAGCCCT 1920
CACTGATGAA GGGATGGACC 1940