EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-09771 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr10:106086630-106088620 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SP2MA0516.2chr10:106088379-106088396CCACTCCCCGCCCCCTT+6
ZNF263MA0528.1chr10:106088146-106088167TCCCCTTTCTCTCTCTCCACC-6.53
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00742chr10:106084541-106101069Adipose_Nuclei
SE_01164chr10:106086553-106091968Adrenal_Gland
SE_02325chr10:106086850-106094009Astrocytes
SE_04416chr10:106086420-106093009Brain_Anterior_Caudate
SE_06314chr10:106084659-106100825Brain_Hippocampus_Middle
SE_09405chr10:106080342-106094322CD14
SE_15073chr10:106085566-106087017CD4_Memory_Primary_7pool
SE_15073chr10:106087043-106090807CD4_Memory_Primary_7pool
SE_16277chr10:106087830-106090281CD4_Naive_Primary_7pool
SE_17744chr10:106080942-106099533CD4p_CD25-_CD45RAp_Naive
SE_18973chr10:106084830-106099514CD4p_CD25-_Il17-_PMAstim_Th
SE_20297chr10:106081116-106091682CD56
SE_21185chr10:106087929-106090265CD8_Memory_7pool
SE_21905chr10:106087778-106090474CD8_Naive_7pool
SE_22733chr10:106084833-106091284CD8_primiary
SE_26115chr10:106084740-106092852Duodenum_Smooth_Muscle
SE_26588chr10:106086699-106100511Esophagus
SE_29918chr10:106086570-106093891Fetal_Muscle
SE_31767chr10:106086630-106092612Gastric
SE_33254chr10:106087367-106089769H1
SE_35928chr10:106086702-106092418HMEC
SE_37140chr10:106086757-106094576HSMMtube
SE_38084chr10:106083444-106094070HUVEC
SE_40236chr10:106087503-106088483K562
SE_40625chr10:106080428-106100998Left_Ventricle
SE_41898chr10:106087366-106088311LNCaP
SE_42144chr10:106080334-106100956Lung
SE_44192chr10:106086438-106093662NHDF-Ad
SE_44781chr10:106086965-106092097NHLF
SE_45613chr10:106084743-106100882Osteoblasts
SE_46824chr10:106086752-106091415Ovary
SE_47282chr10:106085731-106101028Panc1
SE_48584chr10:106084793-106100937Right_Atrium
SE_49548chr10:106086567-106091855Right_Ventricle
SE_50763chr10:106084795-106092025Sigmoid_Colon
SE_51915chr10:106087190-106091144Skeletal_Muscle_Myoblast
SE_53237chr10:106087001-106091967Small_Intestine
SE_53434chr10:106080815-106094302Spleen
SE_55504chr10:106087866-106090000Thymus
SE_55990chr10:106085780-106092333u87
SE_63125chr10:106067855-106110489Tonsil
SE_63710chr10:106087044-106091954HSMM
SE_64455chr10:106087022-106092174NHEK
SE_67964chr10:106085780-106092333u87
SE_68888chr10:106086526-106089890H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10106087819106088091
Enhancer Sequence
TGAGCATCAT CTGAGACAAC AGGAGCTGGA AGAGGCAAAG AGGGACTCTC CTCTAGAGTA 60
TCTGGAGGGA GTGTGGCCCT GATACCTTGA TCCTGGTCTC CAGAACTGTG AAAATAAATG 120
CCCACTGTCT TAAGCCCTCC TGGTGTGTGG CAACTTGTTA TGGCCACCCC AGGAGACTAC 180
TGCAGTCTCA AAGCGCAATG CACCCTCCTC TCTCCCAGCC AGCTCCCCTC GCTGACCTTC 240
CTCTTGTTGG GGTATCTCCA GTCTCCCCAG CCACCTCTGA CCTGGCCTTT GCTCTGCACC 300
GAAGCCTGGG GATTCCACGT GAGATGGAAT CTCTCTCGTG TGCTGGCCAG CGTAGGCCTT 360
TGGGGTCAGC TCATCTGAGC TCTCCCTAAC ACTCCAAACC CCCAGTTAGC TCCCCAACCC 420
TGCACGTCTC CCCTCCCCAT TTCAAGGGAG TCTTGTTTCC ATGGGACACA AGTCAGCGCT 480
TTAAGAATGT TCAAGGCCTG GCCCAACCAG CCTCAGAGGA CCTCTTGGTT CCCTCTCTGC 540
CTGGCCCGGC CACTTCAGAT CATCTCCTGT CCCCCAGATA GCTCCTGCAC CTCCCCACCA 600
TTCCTGGAAA CATCCATGCT TCACCCCTCT GCTGGCCAAA ACCCTACCCA ACTGACCTCA 660
CAGCAAGCCC ATCTCAGACT CCACCTCCAA GGAGCCTTCC AGGATCCCAA GACAAATCCC 720
TCTTTCTTCC AAGGGATAGG AGAACAGGGG AGGGAGAGGG ACATATGAAT TAGGCCCCAC 780
TGAGTGCACC AGGTACCTCA TGTAGGTCAG GTGGCTCTGT AGATGCACCG GCACACAGCA 840
GGCACCCAAC TGAGGCTGGT CCCATGTGTC TCTATCCTTG AATTATTGCA TTTAACCCAC 900
GCAGCAACCC CGGGGGAGGG GGCCATCAGC CTCATGTCCC TGGCAGGAGC CCAAGGTGCT 960
GAGAGGTGGG GCAATGTGCT CAAGGTCACA CAACAGCCTG GCTCCAGGCC CCGTGTCGCC 1020
CTGGTGTGCC CGACAGCTGC CTCTGTCTTT GTCTTGCCCC ATCACCTTCC TCACTGTGAG 1080
CTCCTCCAGG GCAAGGGCAG GGTCCTGTTT GTCTTTGCAT TCCCCAGAGC AACTGGCATA 1140
GACCTGCGCT CCGTGCTAAG GACACACACT ATCCTGGGGG CCCACAGCTC ACACCATGCA 1200
CTGGAGGCAC CACTTTCACA AGACAGTTCC CCACAAATGC CCACCACTTG CAGGAAGGAT 1260
GCCTCTCCCA CAGCCAGCCT GCAGGGGAAG GTCTCCCTCA GCCTCCAGGA TTCCCATCTC 1320
CGGTTTCTAT GCGTGAATCA CAGTGACAGC AATGCGCCCT CACCACTTCC CGTTGTCCTA 1380
CATTGGCTTG GTCTGGGCTC GTATTCCTCC GAATTTCCCC TAGCCCTGTG GCCGCATCTC 1440
ACCCACAAGG GTGCTGGTTT GGAGAGAGCA TGAATACCCA CCTTGGGGCA GGACATGCCA 1500
GAGTTCCCAA GAGTCGTCCC CTTTCTCTCT CTCCACCCCA TGATCTACAC ACCCCCTGCC 1560
TCCAAGCAGA GCCACAAACG TTCAGGCAAA ACCACACTTT CTCAGTGGGA CAGGGAGGGG 1620
AGGCTGCACG CTTAGACGCA GGCTCTGCAC AATAGCAGAC ACACTGACTC AATGGAAAGG 1680
GGAAGGGACT GGAACAGAAC CGGGAGTAAA CACAAAGGAA AACAAGGAGG GAACAAAGCC 1740
CTCCCTTGGC CACTCCCCGC CCCCTTCCAC TTTCCCCCTT TCACTGAGAA ACTAGGATGG 1800
ATGGAATTAA ATAAAGGGCC AGCACCCAGC AGCCACCTTC TGTTTGACCC CTGGATGGGA 1860
ACAAAGAGAG CCCAGCTTAG AAAGACACTC TGCCTCTAGG AGATGGGGGA GGATGAACCC 1920
CCCAAGGCCT TGTCCACGAC CTCGGAAAGG CTTGTTCCCC ACCTCAGCCT CCCCACCCCA 1980
CTGGTCTCTT 1990