EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-03739 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr10:104419690-104422020 
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
CTGACCCCTA GCCACCCCTC CCCTCAGAAA AATAAAGGCT TGCCGAGCAC GTTGGCTCAT 60
GCCTGGAATC CCAGCAGTTT GAAGGTGGAT GGATCACTTG AGTTCAGGAG TTCAAAACCA 120
GCCTGGGCCA CATGGTGAAA CCCCATCTCT ACTAAAACGA AAAATTAGCC AGGCGTGGTG 180
CCACGGGCCT GTGGTCCTAG CTACTCTGGA GGCTGAAGTG GGAGGATTGC TTGATTGAGG 240
CTGGGAGGTG GAGGTTGCAG TGAGCTGAGA TCTTGCCACT GCACTCCAAC CTGGGCAACA 300
GAGCAAGATC CTGTCTCAAA GAAAAAAAAG AAAAATAAAG ACTTTGGGGC TGGCCAGACC 360
AAACCATAGC CTTGGTCTTG CTAACTGCCT CCGCCTTCCT GCCCTGAGGG AGTAGAGGAT 420
GACTCGGGTG GGGTGGTGGA CCCTTGCTTC ATTGTTCCCC TCCCCAGTGT GGCAGGGAGC 480
CAGGAGCAGT ATGACAACAG CTGGCCTACC CCTTCCCTCC CCGTGCACCT GTTTGGGGCT 540
AAAGGGAGTG GGGAAATGAC TGGAGCACAG TGCCCCTCCA GCCCAGGGTG CAGGATGCCT 600
GGGGGCAGGT GCCGGTGGAC AGTCACTTCA CTCCACTCAA ATCTGCTTCT GTCTCACTGT 660
CCCTTTCTCC AGTTCTCAGG AGCCCTGAGA CATCCCCCGT GCCAAGAGTT GGGAGCCAAG 720
ATAAAAAGCT GCCTAATTTC TTTCCCACTT GGCCTAGTTT TGTTTTGGCT GAGGGGAGAG 780
GCCCTTTCCC CAGGTGCGTC AATCCACTGA GATGTGGAGG GGACATTCTG GTGGGAATGG 840
GATGGGCTTG AGCCCCTCCA TGTCCCAGCT TTGAAGCCCA CTCCAGACAA TGACACGCTC 900
AGGCACACAT CTATAGGTGA AGCAGCAGCT GCCCAGAGTT GGCTTGGGGG GGGTTCCCTA 960
GGCAGCCAGG GAAGCAGGGA GACGCTAACC CACCCAGCTG TCCCCAGCCA CCCAGCTGTC 1020
CCTGGCTTTG TAGGAGCAGC TGTCACCCAG CTCCCAAAAG GGTCGGGGCA GAGGAGGCCC 1080
AGAAAGAGCT GGGGCTGCCC CAGGGAACAG GCTTATTCAG AAGTCATCGG AGGGGCCTTC 1140
TCTGCCCTGA ACTGGTGGCC CCTTGGAGGG CTGGCTGCAG CCACAGGTGC CCCAGTGCCC 1200
AGCCCTCCCC TCCTGCCTTC CCCCAAAGGC CATCACGCCT CCCCTTTCCG GGAAGGGTTG 1260
GGGATCTGAC CACGTCTCCC TACCCCACAG ACTGGGGCCG ACAGCTCCTG TGGCCCAGAT 1320
GTGCTGAGCC CGCAGCGAGG CCACCGCGAG GGAGTGGGTG GGGGTGGTTT CCTCTGCTGC 1380
CTGCCGGCCC CAGCTCTTTC ATGTTGCCGC CCTCCCCATC CCAGCCCGGA GCCAAGCAGC 1440
TGGGCCGCTC CTGCCCCCTC CCTCGGCCTC GCTCCCAGCT GTCTTTGGGG TGGGGCAGGG 1500
CAGCTGGGGA ACAGCTGCAA GGCAGGAGCC TGGGGGGTGA TGGGTGCCCC CTGCAACTGC 1560
CGGAAACGGT CTTTGGGCCA AGAAGGGAGT CTGAAGGGTG GGGGTGGAGA GGGCGAGGCC 1620
TAGGGGATGA TCGGCTCCAC CCCTTCTCCC AGCGCATCTG GCCAGGAGAC CCCAGCTCAA 1680
AGCCCCCTCC AGCTTCAAAG GGCACCCTGG GGTGGGAGGC AGGAGACGAG GGTGGATGCC 1740
CTGACCCACT GAGTCCGCAC CCCAGGGCCC CTCTCTCCAA GCTGTGACCT CACCTCAGGG 1800
TTCTTAACAG GCCTTGCTAA CACTCTCCCA CTCAGATCCT GTCATTGTCA CCATGGCCTT 1860
CCTAAGACAC CCTCATCTTC TCCCATCCGA GGGTGGGGGA GAACCAATTC GATTCGCAAC 1920
TTCAGGACCC AGGACCCATC TAGCCGCCTG GGGGATTCCC TACCCCACCT CTGCAGCCTG 1980
TAAATTCTGG GGGAGGAGGC CCTGGAGGGA GGATCAGAGG CATGTCCTTC CCCAACCTCC 2040
CACTCTGGCC TACTAAGAAA TGGGAGCAGG GCTGACCCTA TGAAAGTGTG GGAGGTGAAG 2100
GAGCTGGAGT CGTGATTCCT GGGTATCCCC AGACAGACAT CACCACACTA CAGCCCCTCT 2160
TCTAAGGTGA TCCCAGCACT TTGGGAGGCT GAAGCAGGAG GATCCCTTGA TGAGACCAGC 2220
ATGGGCAGTA TAAGGAGATC CTGTCTCTAT AAAAAATTAA AATATTAGGC TGGGCGCGGT 2280
GGCTCATGCC TGTAATCCCA ACACTTTGGG AGGCCAAGGC AAGCAGATCA 2330