EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-04572 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr10:82247860-82248970 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MITFMA0620.2chr10:82248601-82248619GCAAGTCATGTGACCTTT+6.5
MITFMA0620.2chr10:82248601-82248619GCAAGTCATGTGACCTTT-6.5
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00012chr10:82242422-82272741Adipose_Nuclei
SE_04012chr10:82247422-82248770Brain_Anterior_Caudate
SE_06016chr10:82244701-82248839Brain_Hippocampus_Middle
SE_09209chr10:82243703-82266302CD14
SE_12039chr10:82243827-82248456CD3
SE_12039chr10:82248847-82249491CD3
SE_12748chr10:82248143-82248269CD34_fetal
SE_14580chr10:82243968-82250344CD4_Memory_Primary_7pool
SE_15608chr10:82244601-82248688CD4_Memory_Primary_8pool
SE_17018chr10:82244041-82248812CD4p_CD225int_CD127p_Tmem
SE_17363chr10:82243778-82255908CD4p_CD25-_CD45RAp_Naive
SE_17861chr10:82243686-82255843CD4p_CD25-_CD45ROp_Memory
SE_18324chr10:82243758-82266083CD4p_CD25-_Il17-_PMAstim_Th
SE_19180chr10:82243671-82250881CD4p_CD25-_Il17p_PMAstim_Th17
SE_20438chr10:82244427-82250324CD56
SE_20998chr10:82246727-82248644CD8_Memory_7pool
SE_21854chr10:82244245-82248547CD8_Naive_7pool
SE_22113chr10:82243962-82249502CD8_Naive_8pool
SE_22394chr10:82243692-82252456CD8_primiary
SE_23916chr10:82247562-82248117Colon_Crypt_2
SE_26561chr10:82244847-82248587Esophagus
SE_31654chr10:82247115-82248308Gastric
SE_40835chr10:82246689-82248335Left_Ventricle
SE_42164chr10:82244831-82248731Lung
SE_42164chr10:82248779-82252243Lung
SE_50150chr10:82244670-82248747Sigmoid_Colon
SE_52532chr10:82244801-82248680Small_Intestine
SE_53353chr10:82244672-82249697Spleen
SE_55160chr10:82247691-82248458Thymus
SE_58559chr10:82213055-82265607Ly1
SE_62319chr10:82212748-82296810Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr108224800082248400
Number: 1             
IDChromosomeStartEnd
GH10I080483chr108224287882252356
Enhancer Sequence
GCTGTGTTAC TCTCCTCACC TGGGAAGTGG GGGGTGAGCA GGGGGCTGGC ATGGGACCAC 60
TGCCCTACGG GCCTCTGATC CTGTCCCTAC CTGTGCACTT GAGGCACTCC CTCCTTCCCC 120
ACTGTTCAGC CACTGCATTG GGGGCAGGGG ACCGTGGAGG ACTTCGGGGT CCACCTGGAT 180
TGCCACTGGG GTTCAAAAAG GAAAGCAGCA AAGGTAGGCC AGGCCCTCAG AAAAGTCCCT 240
CGGAAATAGC ACCCTCCTGC AGTAGGATCT CTGAGGTTGC TTTGAGGGTT AGACACAGAT 300
AAAAAACAGT GGCCCCACCC TTCACTCTGT AGTTCACAGG GTCTTCCCAC ATAGGCTGTG 360
TAATCCAAGC TTCATTACAG CCCTGGAGGA CAAAGCTATG GCTATAGTCT GGGTTGAGGT 420
GGAGTGGGGG GCGAGTGACA GGGGAGGGAG GGAGCAGGGG GATGGCTGCT GGCTGCAGTG 480
GCCTTCCTCA CCTCTGAGGG CTGAGCTTCA GAGGTTTTCA GAAAATGTTG CATGAATGAG 540
TATGGAGTCC TCATCTTGGC TTTTCTTCAC TGGGCACAGT TGGATCATGT CCAGACCTGC 600
CTGCACGTTC ATCTCCCAAA CATGGCTCTT TGTGGTCAAG CCCGTTTCTT CTGTTGGCTC 660
TGGTGGGTGG AAAGAACGTG GACTGTGAAG TCCCCTGTCC TTGGTTCCAA TCCTGGGCTG 720
TCATTGCTCT CTTGTCCTTG GGCAAGTCAT GTGACCTTTC TGAATGGTTT CCTCAACCAT 780
GAAGTGGAAA AAAATCAATT CCCAATCGAG AGGTGATGAG ATCAATATTT GGGAAGGCTC 840
CAAGCCGAAT TTCTGGTACT TAGAAGACAC TTAAAAAGCA TCTTTCTTCC TTTCAAAAAT 900
CTCCCTTATC CTTTCGTTTG TCTTTTGGAG AGCTGATTTA ACCTGAGTTT TGCATTACCT 960
ATACCTGGCC TTGGTATCAG GCCTCTGCTT GGACCAGTAA AGGGTCATGA GGGAAATGAT 1020
CGGGAGCTTT CTAGAATCCG CATATGAGCT GGTTTGGGGG AAAGGTTTTA ACGCTGAGCC 1080
TGCCATCTCA CTAGTCACAC ATCTCTCCGC 1110