EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS157-02021 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr10:104419600-104421930 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:104420893-104420911CCTCCCCTCCTGCCTTCC-6.52
INSM1MA0155.1chr10:104420285-104420297TGCCTGGGGGCA+6.04
Myod1MA0499.1chr10:104420724-104420737AGCAGCTGTCACC+6.41
Myod1MA0499.1chr10:104421196-104421209GGGAACAGCTGCA-6.98
SNAI2MA0745.2chr10:104420213-104420223TGCACCTGTT-6.02
ZNF263MA0528.1chr10:104420892-104420913CCCTCCCCTCCTGCCTTCCCC-6.13
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00959chr10:104420854-104421516Adrenal_Gland
SE_03928chr10:104419982-104421719Brain_Anterior_Caudate
SE_04957chr10:104419949-104421554Brain_Cingulate_Gyrus
SE_05850chr10:104419953-104422142Brain_Hippocampus_Middle
SE_06794chr10:104420308-104421508Brain_Hippocampus_Middle_150
SE_07900chr10:104419649-104421175Brain_Inferior_Temporal_Lobe
SE_12288chr10:104420050-104421428CD3
SE_14923chr10:104420080-104421867CD4_Memory_Primary_7pool
SE_17681chr10:104419681-104421932CD4p_CD25-_CD45RAp_Naive
SE_18133chr10:104419610-104422076CD4p_CD25-_CD45ROp_Memory
SE_19041chr10:104419944-104422038CD4p_CD25-_Il17-_PMAstim_Th
SE_19414chr10:104420035-104422247CD4p_CD25-_Il17p_PMAstim_Th17
SE_20458chr10:104419970-104421992CD56
SE_21775chr10:104419870-104420884CD8_Naive_7pool
SE_22797chr10:104419903-104422097CD8_primiary
SE_23338chr10:104419990-104421715Colon_Crypt_1
SE_23909chr10:104420007-104421824Colon_Crypt_2
SE_24984chr10:104420046-104421676Colon_Crypt_3
SE_26660chr10:104420250-104421905Esophagus
SE_29601chr10:104419904-104422066Fetal_Muscle
SE_31097chr10:104419904-104421866Fetal_Thymus
SE_31421chr10:104415469-104421974Gastric
SE_36963chr10:104419171-104422446HSMMtube
SE_41790chr10:104420028-104420406LNCaP
SE_42120chr10:104415488-104421991Lung
SE_44897chr10:104420217-104421082NHLF
SE_50092chr10:104419821-104422066Sigmoid_Colon
SE_52411chr10:104419864-104422065Small_Intestine
SE_53301chr10:104419901-104422036Spleen
SE_55138chr10:104419946-104421398Thymus
SE_62334chr10:104369841-104439105Tonsil
SE_65286chr10:104419766-104421916Pancreatic_islets
SE_66695chr10:104421157-104421796Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10104420025104421916
chr10104420109104421849
Number: 1             
IDChromosomeStartEnd
GH10I102659chr10104419656104421945
Enhancer Sequence
TCGTGCCACT GCACTGCAGC CTGGGTGACA GAGCCAGACT CCATCTCAAA AAAAAAAAAA 60
AAAAGTCCCA TGCCAGTGGT CCAAGCCTCA CTGACCCCTA GCCACCCCTC CCCTCAGAAA 120
AATAAAGGCT TGCCGAGCAC GTTGGCTCAT GCCTGGAATC CCAGCAGTTT GAAGGTGGAT 180
GGATCACTTG AGTTCAGGAG TTCAAAACCA GCCTGGGCCA CATGGTGAAA CCCCATCTCT 240
ACTAAAACGA AAAATTAGCC AGGCGTGGTG CCACGGGCCT GTGGTCCTAG CTACTCTGGA 300
GGCTGAAGTG GGAGGATTGC TTGATTGAGG CTGGGAGGTG GAGGTTGCAG TGAGCTGAGA 360
TCTTGCCACT GCACTCCAAC CTGGGCAACA GAGCAAGATC CTGTCTCAAA GAAAAAAAAG 420
AAAAATAAAG ACTTTGGGGC TGGCCAGACC AAACCATAGC CTTGGTCTTG CTAACTGCCT 480
CCGCCTTCCT GCCCTGAGGG AGTAGAGGAT GACTCGGGTG GGGTGGTGGA CCCTTGCTTC 540
ATTGTTCCCC TCCCCAGTGT GGCAGGGAGC CAGGAGCAGT ATGACAACAG CTGGCCTACC 600
CCTTCCCTCC CCGTGCACCT GTTTGGGGCT AAAGGGAGTG GGGAAATGAC TGGAGCACAG 660
TGCCCCTCCA GCCCAGGGTG CAGGATGCCT GGGGGCAGGT GCCGGTGGAC AGTCACTTCA 720
CTCCACTCAA ATCTGCTTCT GTCTCACTGT CCCTTTCTCC AGTTCTCAGG AGCCCTGAGA 780
CATCCCCCGT GCCAAGAGTT GGGAGCCAAG ATAAAAAGCT GCCTAATTTC TTTCCCACTT 840
GGCCTAGTTT TGTTTTGGCT GAGGGGAGAG GCCCTTTCCC CAGGTGCGTC AATCCACTGA 900
GATGTGGAGG GGACATTCTG GTGGGAATGG GATGGGCTTG AGCCCCTCCA TGTCCCAGCT 960
TTGAAGCCCA CTCCAGACAA TGACACGCTC AGGCACACAT CTATAGGTGA AGCAGCAGCT 1020
GCCCAGAGTT GGCTTGGGGG GGGTTCCCTA GGCAGCCAGG GAAGCAGGGA GACGCTAACC 1080
CACCCAGCTG TCCCCAGCCA CCCAGCTGTC CCTGGCTTTG TAGGAGCAGC TGTCACCCAG 1140
CTCCCAAAAG GGTCGGGGCA GAGGAGGCCC AGAAAGAGCT GGGGCTGCCC CAGGGAACAG 1200
GCTTATTCAG AAGTCATCGG AGGGGCCTTC TCTGCCCTGA ACTGGTGGCC CCTTGGAGGG 1260
CTGGCTGCAG CCACAGGTGC CCCAGTGCCC AGCCCTCCCC TCCTGCCTTC CCCCAAAGGC 1320
CATCACGCCT CCCCTTTCCG GGAAGGGTTG GGGATCTGAC CACGTCTCCC TACCCCACAG 1380
ACTGGGGCCG ACAGCTCCTG TGGCCCAGAT GTGCTGAGCC CGCAGCGAGG CCACCGCGAG 1440
GGAGTGGGTG GGGGTGGTTT CCTCTGCTGC CTGCCGGCCC CAGCTCTTTC ATGTTGCCGC 1500
CCTCCCCATC CCAGCCCGGA GCCAAGCAGC TGGGCCGCTC CTGCCCCCTC CCTCGGCCTC 1560
GCTCCCAGCT GTCTTTGGGG TGGGGCAGGG CAGCTGGGGA ACAGCTGCAA GGCAGGAGCC 1620
TGGGGGGTGA TGGGTGCCCC CTGCAACTGC CGGAAACGGT CTTTGGGCCA AGAAGGGAGT 1680
CTGAAGGGTG GGGGTGGAGA GGGCGAGGCC TAGGGGATGA TCGGCTCCAC CCCTTCTCCC 1740
AGCGCATCTG GCCAGGAGAC CCCAGCTCAA AGCCCCCTCC AGCTTCAAAG GGCACCCTGG 1800
GGTGGGAGGC AGGAGACGAG GGTGGATGCC CTGACCCACT GAGTCCGCAC CCCAGGGCCC 1860
CTCTCTCCAA GCTGTGACCT CACCTCAGGG TTCTTAACAG GCCTTGCTAA CACTCTCCCA 1920
CTCAGATCCT GTCATTGTCA CCATGGCCTT CCTAAGACAC CCTCATCTTC TCCCATCCGA 1980
GGGTGGGGGA GAACCAATTC GATTCGCAAC TTCAGGACCC AGGACCCATC TAGCCGCCTG 2040
GGGGATTCCC TACCCCACCT CTGCAGCCTG TAAATTCTGG GGGAGGAGGC CCTGGAGGGA 2100
GGATCAGAGG CATGTCCTTC CCCAACCTCC CACTCTGGCC TACTAAGAAA TGGGAGCAGG 2160
GCTGACCCTA TGAAAGTGTG GGAGGTGAAG GAGCTGGAGT CGTGATTCCT GGGTATCCCC 2220
AGACAGACAT CACCACACTA CAGCCCCTCT TCTAAGGTGA TCCCAGCACT TTGGGAGGCT 2280
GAAGCAGGAG GATCCCTTGA TGAGACCAGC ATGGGCAGTA TAAGGAGATC 2330