EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS182-00354 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr1:19791120-19793570 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RESTMA0138.2chr1:19792759-19792780GGAGCTATTCAAGGTCCTGCC-6.03
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00361chr1:19790977-19793327Adipose_Nuclei
SE_01199chr1:19791256-19791923Adrenal_Gland
SE_01199chr1:19791954-19793061Adrenal_Gland
SE_02919chr1:19791727-19794492Bladder
SE_05833chr1:19791940-19793473Brain_Hippocampus_Middle
SE_09593chr1:19791004-19793426CD14
SE_10714chr1:19788847-19792129CD19_Primary
SE_12250chr1:19791044-19793211CD3
SE_13780chr1:19791133-19792561CD34_Primary_RO01536
SE_14589chr1:19782676-19793243CD4_Memory_Primary_7pool
SE_17553chr1:19780030-19800464CD4p_CD25-_CD45RAp_Naive
SE_18042chr1:19782765-19793570CD4p_CD25-_CD45ROp_Memory
SE_18410chr1:19788739-19800215CD4p_CD25-_Il17-_PMAstim_Th
SE_19269chr1:19791285-19793280CD4p_CD25-_Il17p_PMAstim_Th17
SE_21829chr1:19791177-19793536CD8_Naive_7pool
SE_22220chr1:19790956-19793691CD8_Naive_8pool
SE_22607chr1:19787028-19798132CD8_primiary
SE_25786chr1:19791024-19792824Duodenum_Smooth_Muscle
SE_26537chr1:19791062-19797219Esophagus
SE_28668chr1:19791416-19796928Fetal_Intestine_Large
SE_31447chr1:19791409-19791965Gastric
SE_31447chr1:19792007-19796937Gastric
SE_42185chr1:19791568-19793297Lung
SE_45720chr1:19791124-19792736Osteoblasts
SE_46635chr1:19791599-19791992Ovary
SE_46635chr1:19792035-19793295Ovary
SE_47234chr1:19791648-19796693Panc1
SE_50058chr1:19791076-19798191Sigmoid_Colon
SE_51211chr1:19791343-19792689Skeletal_Muscle
SE_52345chr1:19791184-19797955Small_Intestine
SE_54550chr1:19792004-19793080Stomach_Smooth_Muscle
SE_62519chr1:19761354-19815005Tonsil
SE_65446chr1:19792071-19793267Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11979130719791453
chr11979173119791982
chr11979204319792168
Enhancer Sequence
CATCCAAAAA CTGGAGGCAA CCCAAATGTT CATCAACTGC TGAATGGTAC GTCCATACCA 60
TGGAATACTA TGGAATGCTC TACAGCAAGA AAAGGAAATA TTAATACATG CAACATGAAT 120
GAATCAAATA AATCATGTTA CACGAAAGAG GTCAAACACA AAAGACTCCA TACTATCTGC 180
TTCCATTTAT TTACAATTAT AGAAAAGGCA AAACCGCGGT GACAAAGCAG ATCAGTGGTT 240
GTCTAGGGAT GGGGAACAAG GCTGTCTAGG AGGGGGAAAA GGGCCAAAGG GGCATGAAGG 300
GACTTTTTAG GGTGAGGAAA CTGTTCTATA ACTCGATTGT GGTGGTGGCA ACATGATTAG 360
TACCAAAACT CAAACTGTAC ACTTAAAGCT GGTTAATTTT ATTACTTGCA AATAATACCC 420
TGATTAAAAA CAAAAAAAAG AAGACCCTAG AAATCTTAGC TGTGGTTGGC AGGGGAGAGT 480
GGAAGACACT GGGCATGTGA GAAGAGAAGG CAGTGTTTTA TGTGTGTTGT GGTCTGAATG 540
CTGGTACCCC CTCAAAATTC ATATGCTGAA ACATAATCCC CAATGCCAGA GTTAAGAGGT 600
GAGGCCTTTA AGAGGTGATT AGATCATGAG GGCCCCACCT TCATGAATGA CATTAATGCC 660
CCTATAAGAG GCCCAGGGGA GCTGGCCAGC CCCTTCCACC ATGTGAGGCG CTGTCTATGA 720
TGCAGAGAAC AAGCCTTTGC CAAACACTGA GTCTGCCAAG ACCTTGCTTA CGGACTTCCC 780
AGCCTTCAGA ACTGTGAGTA ATCAATTTCT GTTGTGTACA AATTATTCAG TTTAAGGTAT 840
TTGTTCCAGG AGCCCAAACA GACTAAGACA ATGTATATAT TTTTATTTTT GAAACCTGTG 900
ACTGAATTGC CTATTCCAAA CTTGAGCTCT AATTCTTTCA AAGCCAACTG CAGAGGTGAC 960
TCTGTGCAAT GGCTCAGGTA GAAGTGGTGT GGTCCATTGC TGGGTTCCTG TTGGTCAGGG 1020
ATATAGGCAC CAAAAGCTTA GAGGGTGGGG AGAATGAAAA CCTCTGGATC TAACCAGAGC 1080
TGAATGTAGA AAACCATCTA TCTCCTCTCC TCCCAGAAGC CAGTGCCTCC TGTCCTGGGC 1140
CTCTGGGCTC ATGTGATAAA GACAAGAGCT ACCATTTATT GGGCACTTAC TATGTCCCAG 1200
GTGCTACGAC TCATTTGACG TGCATTAACT CATTAACAGT GATAAGACCA ACAACATGTA 1260
CGGAGCCCTA TATGTGCTAG GTATGACAGG CCTTCTTACC TGCTTGACCT CATTTAATTA 1320
GCCTCAAATC GATCCTATGA CAAGGAACCA GTCCCAGAGA GTTAAGTGAA GCCCAAGGCT 1380
ACACAGCTAA AAGTGTAAGG GAACAAAGAT TTAAACCCAG GCAGTCTGGC CCCAGGAGCC 1440
CAGCTACCAT CCATGACCAA GGACAACCCT TTTATTGGGA CAGAGGCGAC ACTAATCACT 1500
GCACGCACTT AGGCTGAGGT GTGGTGGGTG GAGGATCAGA CTCAGAGGTG AATCTGTGCT 1560
CCTGGCCTAC TCCACCAGCT CCACAGCTCC GCCAGGAGGG TCTTTCACTC CCACACTGGG 1620
GAGGCAGAGC CAGATGCATG GAGCTATTCA AGGTCCTGCC TAGCTCCAAA GCCCTTACTC 1680
TTTGCACTAG ACCAGGCTGC TTCCTTGGCT AATAAACAGT GAGAGCTGAA ACCCAAACAA 1740
AAACAAGCAG CACACGTGAA GACAAAATGT TCCTGAGCTG CAACGTTTTT CAATCTTTTG 1800
AGCTCATAGA TCACATGTCT AGGTCAGAGT CCTGAGCTTC CTCACGGCGC AGGTGATGTG 1860
AGAGGGGCTG AGTAACCTCG AGGTACCACT GAATGGCATC CTGCAGTCAC TCAAAACGTG 1920
TGAGCCTGGA GGGACCCTGG TGCTCACATG GTCTGATATG CAAAGAAGAA AAAGAGGCAT 1980
GGGGGATCGG GAATAGTTCA ACATCACCCA GCACATCAGA GGCCAGGATG CAGTCCCAAG 2040
TCACGCTCCA GACTCCTGGT ACAGTGCTCT TTTCACGCCT GCAGCATTTC CCATGGCATG 2100
CTGTGCAGGC CAATGGGGTT TAAGGGAGGT TTTAGAGAGC ATATGGATGA ATGCAGTTTA 2160
ATAATTACCT ATATTTAATA TTCATAGGAA AAATATAACT AGCACATCAA ACATGATTTT 2220
GTAGATGTTT CTGCTTACGA AGAGGCTAGA TAGCGGTGTT AGGCTCAGGC CAAAGTTTTT 2280
TGTTTTTGTT TTTGAGAGAG GGTGTTGTTC TGTCACCCAG GCTGGAATGC AGGAGTTATT 2340
CATAGGAAAA ATCCTAACAC ACAAGCTCCA GGGATCCTCC CGCCTCAGCC TCCCAAGTAG 2400
CTGGGACTCC AGATGCACCA TCACACCCAG CTTTTATTTA TTTATTTATT 2450