EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-04787 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr10:104420000-104421840 
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
Number: 1             
IDChromosomeStartEnd
GH10I102659chr10104419656104421945
Enhancer Sequence
CTGTCTCAAA GAAAAAAAAG AAAAATAAAG ACTTTGGGGC TGGCCAGACC AAACCATAGC 60
CTTGGTCTTG CTAACTGCCT CCGCCTTCCT GCCCTGAGGG AGTAGAGGAT GACTCGGGTG 120
GGGTGGTGGA CCCTTGCTTC ATTGTTCCCC TCCCCAGTGT GGCAGGGAGC CAGGAGCAGT 180
ATGACAACAG CTGGCCTACC CCTTCCCTCC CCGTGCACCT GTTTGGGGCT AAAGGGAGTG 240
GGGAAATGAC TGGAGCACAG TGCCCCTCCA GCCCAGGGTG CAGGATGCCT GGGGGCAGGT 300
GCCGGTGGAC AGTCACTTCA CTCCACTCAA ATCTGCTTCT GTCTCACTGT CCCTTTCTCC 360
AGTTCTCAGG AGCCCTGAGA CATCCCCCGT GCCAAGAGTT GGGAGCCAAG ATAAAAAGCT 420
GCCTAATTTC TTTCCCACTT GGCCTAGTTT TGTTTTGGCT GAGGGGAGAG GCCCTTTCCC 480
CAGGTGCGTC AATCCACTGA GATGTGGAGG GGACATTCTG GTGGGAATGG GATGGGCTTG 540
AGCCCCTCCA TGTCCCAGCT TTGAAGCCCA CTCCAGACAA TGACACGCTC AGGCACACAT 600
CTATAGGTGA AGCAGCAGCT GCCCAGAGTT GGCTTGGGGG GGGTTCCCTA GGCAGCCAGG 660
GAAGCAGGGA GACGCTAACC CACCCAGCTG TCCCCAGCCA CCCAGCTGTC CCTGGCTTTG 720
TAGGAGCAGC TGTCACCCAG CTCCCAAAAG GGTCGGGGCA GAGGAGGCCC AGAAAGAGCT 780
GGGGCTGCCC CAGGGAACAG GCTTATTCAG AAGTCATCGG AGGGGCCTTC TCTGCCCTGA 840
ACTGGTGGCC CCTTGGAGGG CTGGCTGCAG CCACAGGTGC CCCAGTGCCC AGCCCTCCCC 900
TCCTGCCTTC CCCCAAAGGC CATCACGCCT CCCCTTTCCG GGAAGGGTTG GGGATCTGAC 960
CACGTCTCCC TACCCCACAG ACTGGGGCCG ACAGCTCCTG TGGCCCAGAT GTGCTGAGCC 1020
CGCAGCGAGG CCACCGCGAG GGAGTGGGTG GGGGTGGTTT CCTCTGCTGC CTGCCGGCCC 1080
CAGCTCTTTC ATGTTGCCGC CCTCCCCATC CCAGCCCGGA GCCAAGCAGC TGGGCCGCTC 1140
CTGCCCCCTC CCTCGGCCTC GCTCCCAGCT GTCTTTGGGG TGGGGCAGGG CAGCTGGGGA 1200
ACAGCTGCAA GGCAGGAGCC TGGGGGGTGA TGGGTGCCCC CTGCAACTGC CGGAAACGGT 1260
CTTTGGGCCA AGAAGGGAGT CTGAAGGGTG GGGGTGGAGA GGGCGAGGCC TAGGGGATGA 1320
TCGGCTCCAC CCCTTCTCCC AGCGCATCTG GCCAGGAGAC CCCAGCTCAA AGCCCCCTCC 1380
AGCTTCAAAG GGCACCCTGG GGTGGGAGGC AGGAGACGAG GGTGGATGCC CTGACCCACT 1440
GAGTCCGCAC CCCAGGGCCC CTCTCTCCAA GCTGTGACCT CACCTCAGGG TTCTTAACAG 1500
GCCTTGCTAA CACTCTCCCA CTCAGATCCT GTCATTGTCA CCATGGCCTT CCTAAGACAC 1560
CCTCATCTTC TCCCATCCGA GGGTGGGGGA GAACCAATTC GATTCGCAAC TTCAGGACCC 1620
AGGACCCATC TAGCCGCCTG GGGGATTCCC TACCCCACCT CTGCAGCCTG TAAATTCTGG 1680
GGGAGGAGGC CCTGGAGGGA GGATCAGAGG CATGTCCTTC CCCAACCTCC CACTCTGGCC 1740
TACTAAGAAA TGGGAGCAGG GCTGACCCTA TGAAAGTGTG GGAGGTGAAG GAGCTGGAGT 1800
CGTGATTCCT GGGTATCCCC AGACAGACAT CACCACACTA 1840