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

TagContent
EnhancerAtlas ID
HS134-13916 
Organism
Homo sapiens 
Tissue/cell
Mesendoderm 
Coordinate
chr12:65062630-65064140 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr12:65063350-65063371ATTCAGTTTCTCTTTTTCTTT+7.56
IRF9MA0653.1chr12:65062975-65062990AGTTTCTGTTTTGTT-6.02
ZNF263MA0528.1chr12:65063578-65063599GGAGGAAAAGGAGCTGGAGGG+6.25
ZfxMA0146.2chr12:65062692-65062706CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01804chr12:65062857-65064095Aorta
SE_11789chr12:65048359-65079116CD20
SE_11913chr12:65058342-65070092CD3
SE_14822chr12:65058251-65070120CD4_Memory_Primary_7pool
SE_15696chr12:65061649-65064764CD4_Memory_Primary_8pool
SE_15988chr12:65062515-65064569CD4_Naive_Primary_7pool
SE_16487chr12:65061093-65065642CD4_Naive_Primary_8pool
SE_17278chr12:65061350-65064143CD4p_CD225int_CD127p_Tmem
SE_18102chr12:65057726-65070402CD4p_CD25-_CD45ROp_Memory
SE_18758chr12:65058416-65080356CD4p_CD25-_Il17-_PMAstim_Th
SE_20172chr12:65058509-65070241CD56
SE_21231chr12:65061300-65065883CD8_Memory_7pool
SE_21679chr12:65061360-65065973CD8_Naive_7pool
SE_22024chr12:65058680-65070332CD8_Naive_8pool
SE_22370chr12:65057844-65080308CD8_primiary
SE_26327chr12:65062514-65065978Duodenum_Smooth_Muscle
SE_32113chr12:65062934-65064196Gastric
SE_35199chr12:65062724-65070283HeLa
SE_41405chr12:65059183-65065857Left_Ventricle
SE_41811chr12:65062952-65063809LNCaP
SE_41811chr12:65063848-65064135LNCaP
SE_43200chr12:65062758-65065840Lung
SE_49372chr12:65062833-65063696Right_Atrium
SE_49372chr12:65063828-65064115Right_Atrium
SE_50736chr12:65062629-65065852Sigmoid_Colon
SE_54802chr12:65062503-65065859Stomach_Smooth_Muscle
SE_57296chr12:65063275-65063655VACO_400
SE_59758chr12:65002038-65072203Ly4
SE_63011chr12:65051055-65082906Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr126506266065064122
Number: 1             
IDChromosomeStartEnd
GH12I064664chr126505818265079989
Enhancer Sequence
TTTTGTATTT TTAGTAGAGA TGGGGTTTCA CCGTGGTCTC GATCTCCTGA CCTCGTGATC 60
TGCCCGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCTACCGC ACCCAGCCCA 120
ATTTTGATTT TTTAGGAGGA AAAAAAATTG TTCCTAAGGA AGTCAAGTCC TAAATTGAAA 180
GACTTTCATA TATTACACAA ACCCTAGAAA AACTTGGGTT ACACCTGGGA TTGATTTTGA 240
AGTAGGGCGT TGAACTATGT GTCCTGTTTA ACCTCGAGGA GCAAATGGCT TTCCATTCTA 300
AACATTCTCA TTTCTTCTCT GGGACATTCT TTAGGTGCTT GTTTGAGTTT CTGTTTTGTT 360
AGGCACATTA GAGGACTCTA TATGAACAAG TTCCTAGGGG AGGAAATTGG TGACTTAGAT 420
GAAAGGGTGA AAAAGGTGAA ACCTTCACAT TATTGTGTAA GGGATTGTCC CAGAATGTGT 480
GAAATTTGAT GTAGTCCTTC TTGGCTTCGT TTTTTCCTCA GATGTTCTGG ATGAAACAGT 540
TCCCCCTGTC ACACGTGGAG ATAAGGATGT GGCTCTAGGC AGGGCATATC CTGTGTTTAA 600
GACTGTGTTG ACTCTTCTTT TACAGTGTCT GCCACTTGTT TCCTGCCTAG GTCTTTAGTT 660
TTGAGTGAAG TACAGCTGTG AAGTCCTAGA CTTGTAATGC TAAGGCGTTC ATTATGTTAA 720
ATTCAGTTTC TCTTTTTCTT TTCTCTGCTT CACATCAGCC TTGTACTTTA GCACGTTTCC 780
AGTCCAGCCT TGGTAGCTGG GCTGCTGTTC TCCTTGACCC GTCCCTTTGC AAGCAGCAGA 840
CCACGGCCAG GGTTGGGAGT CCGGCTGGGC CACTGACCGC AGTGCTGAGG AAAGGTGGAG 900
CGGGAGGCCC TTTCCTCCCA GCCTCGGGCT TCCTGTGCAA GCCACTGAGG AGGAAAAGGA 960
GCTGGAGGGT GTGTGAACCC TCAGGTTATA CAAGCAGCAC TTCTATGCAA CAAAGAAAAT 1020
GTAAATTGCT GTAAATTACC AAAAAAAAAA AAAAAAAAAA AATTGCTGGC AATCTGCTTT 1080
CCAGGGCAGA TGGAGGGTAG CTTTTATTTA TACATTGGTC AGCTGATTGA GTAATGTTTA 1140
AAAACCACCT TTACTTCTGG CACTTCTTGG CAGTATCAGT TTTTTTTTTT TAATGGATAG 1200
AGAAGCTTTT TTATTTTACA GATAATAACT GCATATCTTT ACCTGAGGGA GCTCAGGTTC 1260
GCTCTATCTA GCAGCTTCCA CGTGTCATCT CTGTATGTGC AGTTGGTGCC TGCATTAAGG 1320
AGGACGGACA GCCTTGTGGC GTTGGTGCCT CTGTTTTGTG TCTAAAGCTA TTTATTTGGG 1380
GGTGGCTGCC CCAGGAGCAG CACATCAAAG TGGTGTTCAG TTATGCTGGC CAAGTGCTGA 1440
ATTGCATTGT GTTTATTTTT ATTTCCAAGG TTATTTTATT TTTTACACAT GAAAGCCTTT 1500
TTCCCTCCTA 1510