EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-09828 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr22:37630910-37633100 
Target genes
Number: 9             
NameEnsembl ID
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr22:37632080-37632097GGGAACACAGAGTTCCT+6.02
ZNF143MA0088.2chr22:37631714-37631730TGAGGCATGATGGGAA-6.05
ZNF263MA0528.1chr22:37631393-37631414TCCTTCCTCTCTCCCTTCTCT-6.31
ZNF263MA0528.1chr22:37631399-37631420CTCTCTCCCTTCTCTTCCTCC-7.25
ZNF263MA0528.1chr22:37631402-37631423TCTCCCTTCTCTTCCTCCCCA-7.37
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_09557chr22:37629393-37634416CD14
SE_10320chr22:37630298-37634369CD19_Primary
SE_11141chr22:37613444-37642817CD20
SE_11906chr22:37629612-37636176CD3
SE_14617chr22:37630213-37636272CD4_Memory_Primary_7pool
SE_15906chr22:37631030-37632999CD4_Naive_Primary_7pool
SE_16510chr22:37631102-37632710CD4_Naive_Primary_8pool
SE_16969chr22:37631698-37633075CD4p_CD225int_CD127p_Tmem
SE_17369chr22:37612712-37642072CD4p_CD25-_CD45RAp_Naive
SE_17862chr22:37613647-37642207CD4p_CD25-_CD45ROp_Memory
SE_18463chr22:37621942-37642050CD4p_CD25-_Il17-_PMAstim_Th
SE_19164chr22:37629500-37641686CD4p_CD25-_Il17p_PMAstim_Th17
SE_20119chr22:37629579-37642292CD56
SE_21034chr22:37630028-37632567CD8_Memory_7pool
SE_21592chr22:37630015-37632629CD8_Naive_7pool
SE_22062chr22:37629383-37636130CD8_Naive_8pool
SE_32637chr22:37631607-37632963GM12878
SE_50312chr22:37629549-37633009Sigmoid_Colon
SE_53490chr22:37630044-37633057Spleen
SE_55137chr22:37629533-37632167Thymus
SE_55137chr22:37632305-37632969Thymus
SE_55695chr22:37631791-37632839u87
SE_58850chr22:37613664-37681838Ly3
SE_60812chr22:37614284-37642429DHL6
SE_61227chr22:37613918-37681610HBL1
SE_62378chr22:37613614-37642624Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223763266037632962
Enhancer Sequence
TGCCCAGACA AGTCCTCCTC TCTGGCGGAG CTTCGTCGTC CTCTACCTGT AAAGAGCCCA 60
TGGTTCCCTC TCTCAGGTGA CTACTTTGCC TGGACCACGA GCAGGCACTT GGTGAGTCTC 120
CACCCCTTCA AGGGCTGTGG GTTCTGTGTG GGCCAGGCCG ATGCCTGCTT ATTCTCCACA 180
GTCTCAGGCC TGTCACCCAG TGAATGCAGG TGGAAGGGAA TTAAACCACC TCCTCCAGGA 240
AGTCCTCAGA GAACGCTACT CAATGTTAGG CTGCAGAAGC GCTAACACTT CAGAGTAACA 300
CAAAAGACAC CTCTCCTGAG AGGAGTCCCC CACACCCCCA AAAAGTGGGC AGCCCAGCCT 360
TTTTAATACA CTTTGCCTGT CCAGCCCTGG ACAGAATTCC TGGTTACCTC TCAGTTCCTC 420
AAACGGCCCT GTTCCCGCCT GTCTGGAAAG TGCCTGCAAA CAGTGGCCCC TGACTTCCCA 480
CTCTCCTTCC TCTCTCCCTT CTCTTCCTCC CCACTGCCAG GCTGGCTGAC TTTTACTCAT 540
CCCTCCAGCC CCTGCTCAAT GTCACCTCCT CCAAGAAGCC TTTCCTGACT TCCAGCCATG 600
TCGGGGCTAC CACCCCACCT AAACCAGCAC TCCTTGGGGA ACTCAGCATC CCAGGTGGCA 660
GGCACTAAGC CTCATTTGTT TGCCGCTGCA CCCTGGGGCC AGCCCGCGGT CTGGTGCACA 720
GCAGGTGCTG GCGTGCACCT ACTCTGGGTA CCACCTACAC TGCTGTGGGA TTTCAGGAAG 780
AAGGCGCTGT CCAGGGAGAC ACAGTGAGGC ATGATGGGAA AAGCCACACC TGTGTTGTTT 840
TTCCAGTTTT GACCAGAAAC ACACTTTTGG GAAATGCTTG GACACTCTCT CCTCTAATGT 900
CCAGCCACAG TGCTAGTGCC AAGAAGCCCC ACAAGATTCA CCTGTCTCCT CTGGGTCATC 960
CCTGGAATCT CAGGGCCACG GTGATGGGGA AAGAGCTGGG ACCTTGAGAA GCAACAGCCA 1020
CCTTCTCTGA GGCCAGGCAG GGGGCTGAGG GTCTTTGTAT GTTAGGTCTT GAAGTCTCAT 1080
GTGATCCAAG ACAAAAGGAT CTTAAGTTAC CCCCATTAGA CAGATGAGGA AACTGAGGCC 1140
TGAAGAGGTC AAGGACCTTT CTTGTTGGGC GGGAACACAG AGTTCCTTGG GAAGCCAGGA 1200
CATCCTGGCT GTGTGACCCT GGGTGAGTGA CCTAACTTCT CTGAGCCTCA ATCTCTTTAA 1260
TGTGGAGGGG AAAATACCTA TTTCTTGGAG CCATTAGGAG AATCCAAAAA AACAGAGGAT 1320
GTTCAAGCCA CCCCACTGGG AGATGCTGAG AAGCTAAGCA GTCTCATTTT CCATGTCCCC 1380
AAATGCCCCT GCCACAGGGC CCCTCCCCAG AGGACCAGAG GGACAGGTGC AGGAATGTGT 1440
CAATGGTGTG ACACCCCTGA GGGTCCCCCT TACTTAAGAG ACCCACAGGC AGCCAGGACC 1500
AGAGAGGAAC CTTATGCACA GACCACCATG GGCAACCCTC ACCCCATTTT CCGGATGAAG 1560
AAATTGAGGC TTACAGAGAG GAAGGGACTT GCCCAAGATC TCCCAGCCAG TGGGTGGCAG 1620
AGCAAGGCTA GATCCTGTTA CCCAATTCAG AAAGGCCCAC ATGGTAAGCA TCGCTGCTAT 1680
TTCATGGCTG GAAATGGAGT TGGAGAGAGC AGAGACCATG TTTTCATCTA GTGCCTGTAG 1740
AACTCTGAGG CCTGGCCCTA GAATGGAGTG GAGGAGGGGA ATGGGGCAGG TGGAAGGGGC 1800
CCCAGCACCC AGGTATCACC TGACCACCAC CGAAGCCCAC CCCCACGGAG GAAGGATGGT 1860
GCATTCAAGG AACCCAGAGA CCACAGGGCA CGCATGGCTA GTGACTTGGG GGTGAGAAAG 1920
GATTGATGTC ATAGGGGCAC GGACCAGTCA GGTCTTGGTT CTCAGGGCAA TGGGGAACCA 1980
GCAAGGGGCC AAGCCAGGCA GAGGTGATGA GATCAGATTT GCATTTATAA AAGGTCCCAG 2040
CTGGGCACGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCTGAGG CAGGTGGATC 2100
ACCAGGTCAA GAGATCGAGA CCATCCTGGC CAACATGGTG AAACCCTGTC TCTACCAAAA 2160
ATACAAAACT TAGCTGGGTG TGGTGGTGCA 2190