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

TagContent
EnhancerAtlas ID
HS031-23482 
Organism
Homo sapiens 
Tissue/cell
Denditric_cell 
Coordinate
chr8:134088620-134091060 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr8:134090585-134090606AGAGGAAGAGCAGGAGGTGGA+6.12
ZNF410MA0752.1chr8:134090211-134090228CCCATCCCAAAATAAGA+6.05
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_09394chr8:134078239-134096405CD14
SE_11575chr8:134063316-134089541CD20
SE_11927chr8:134064595-134089484CD3
SE_14663chr8:134078035-134089000CD4_Memory_Primary_7pool
SE_16340chr8:134078026-134089043CD4_Naive_Primary_8pool
SE_17447chr8:134061061-134090759CD4p_CD25-_CD45RAp_Naive
SE_17833chr8:134055110-134089450CD4p_CD25-_CD45ROp_Memory
SE_18304chr8:134051801-134090347CD4p_CD25-_Il17-_PMAstim_Th
SE_19149chr8:134077981-134088954CD4p_CD25-_Il17p_PMAstim_Th17
SE_19149chr8:134089089-134090742CD4p_CD25-_Il17p_PMAstim_Th17
SE_20067chr8:134077988-134089543CD56
SE_20915chr8:134078310-134089004CD8_Memory_7pool
SE_21746chr8:134083318-134088890CD8_Naive_7pool
SE_22028chr8:134077933-134089133CD8_Naive_8pool
SE_22419chr8:134061464-134089708CD8_primiary
SE_25356chr8:134063988-134091359DND41
SE_30982chr8:134082198-134089188Fetal_Thymus
SE_30982chr8:134089918-134090808Fetal_Thymus
SE_39451chr8:134085750-134090829Jurkat
SE_50024chr8:134085706-134089527RPMI-8402
SE_50310chr8:134084705-134088943Sigmoid_Colon
SE_50310chr8:134088993-134091015Sigmoid_Colon
SE_52872chr8:134082241-134088867Small_Intestine
SE_52872chr8:134088987-134090896Small_Intestine
SE_53656chr8:134082197-134090904Spleen
SE_55122chr8:134089421-134090576Thymus
SE_58475chr8:134064211-134108156Ly1
SE_59938chr8:134066750-134106207Ly4
SE_60964chr8:133960549-134107308HBL1
SE_62289chr8:134055023-134106177Tonsil
SE_66339chr8:134085750-134090829Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr8134090070134090677
chr8134089498134089860
Number: 1             
IDChromosomeStartEnd
GH08I133077chr8134090070134090754
Enhancer Sequence
CCTCAGGGCT GCTTCTAAAT TTAGCAGGCA GGCACTCTGC ACTAGAGAGA TGGTTCCTTA 60
GACAACTTGT GAAAACACCC GCTCAAGAAG AGCATGCTGG GAAGGTACAA AGGAACTATT 120
GCAAAAGACT GAGTGGGCAG TTTGCTTTAC AGGGAAGACG GGATAGGCAG AAATATGCAG 180
AAGTGGAGAT TTTCCCCCAA ATTCACACAG AGGAGTAAAA GAGCTTTAGA CTGATAGTCA 240
GAGGTATGAG TTTTGTGATG ACTTTTTAAT AGACACTTAC CAAGAAAGAA TCTAGTACAG 300
ATGAAGCTCT GAATTTATTC CCTGTCATTT CTTTAGTAAA ACTTTATTGA GCAAGGCATA 360
TTCCACAAAC TGGGATTTAG CTGTAAAAAA AAAAAAAAAA AAAACAACTG CAAAAGCCCT 420
GCCCTTCCCT GTACTTAACT TAATTTAAAG GGGACTACAG AGACATGGCG ACTTGGTGCA 480
AAGTGTGGGT CACGGGAAAA GAACTAGAAA GAACATTATG GGGTGGCGGT TATTTGAATA 540
TGTACTACAC AGCAGATTCT ACTACTTCCC CTAGGAGGAG TCCTATGGGA AAGACTGAAT 600
ATGTGACTAT CAATTATGGC GACCCATCAA AGAAACTCAA TGGGTTGATG GGACCGAGGG 660
GCGCAGATGT GCTACTTTGC ACAGGTGGCC AGTCGTGGGG TGGATGGGCT CTCTCTAGAG 720
ATATCATTAG GCTGAGAACT GTAGGAGGAA AGGAAGCCAG CCCTGGGACA AGCCAGGGCA 780
TGAGAGGTGT GCGCAGAAGG GACTGCTGGT TTCACACAAG CTTTAAAAGT TTTTGGGAAA 840
GACAATCAGC CCTAAAGATG TTCAAGTCAG AGGCAGAGGC AGACAAGAGA GAGGCCCATA 900
GAGTGGGTTC CTGTTCAAGG GGTCCCGTTC ACAGGAGAAG CTACAGAAGA AGGAGAAAGG 960
CAGGATGCAG AGCCCTGGAG GTCAGGGCCG CAGGCTCTTC TCTGTTTTTG TCCAGTGGGT 1020
CATTGGGTGA CTGAAGGGTT GCTGCTAACC TCCCCTGACC CCCAGCCCGG GGTGTTTATG 1080
ACCCTCCCTT TCGCCTCCTG GAGTAACCGA GGAAACTTAG TAGGTTTGAG AAAGTGTTCC 1140
TCATACTGGG CACTGTGCTA TCCCAAAGCC TGGGCTGTGC CAGAGCAGGG GGATGGAATG 1200
GAGGTTTTGG CCCTGGGCCC AACCAGAGAC GGCAGGGCTG AAGCCCGATG CCACGCTAGA 1260
CAGGTGACTC AAATCTTAGG CCTCTGTTTT CAGTAACCCC AAGCGGGGTC TCAGCCTCAG 1320
CACTTTGGAC ATTTTGGATC AGGGCATTCT CTGGTGTGTA TGTGTGTGTG TGTGTGTGTG 1380
TGTGTGTGTG TTTGTATGTG TGTGTGTGCG GCAGAGTTGC AGGGCTGACC TGTGCATTGG 1440
AGGATGTGCC ACAGCATCTC TGGACCTGAC CCCCTAGACA GCAGGAGCCC CCCGCACCCC 1500
TCCAAGTCAT GACAACCAAA AATGTCCCAG AAATTGTCAA ATGTGCCCTA GGGAGCAAAA 1560
ATTGCCCCCA GTTGAGAACC ACTGGATCAT ACCCATCCCA AAATAAGACA CGTGTGAAGG 1620
TTGTTCTTTC TTGGGTTGTA AAGTGCTGCC CTGAGGGCAG TTGGTTTTCC TGCTTTTGTG 1680
TGGACTCAGC TCTGCAGCAC GTCTGCCTGT GCTCTCTGGT ACACATCTAA GAAGCTGCTG 1740
TGTAGCAAGG CTCCTTTGGG TGGCTGTGTC ACCCATCCTT CCTCTCCACC ATCATACACG 1800
TGACCCAAGA AGAGGAACTG GTTTGTGGTC TGTTCAGGAG TCCCTGGGAA TTAGGGCTTG 1860
GAAGCTACAG TATGGGCAGC CTGTGAGCTG CATCTTAAAG GAGGAGCAGT TTGCTGTCAA 1920
GAACTGGGGT GGGAGCATGT GAGCCACGAG CTGCCTAAGG ACAGGAGAGG AAGAGCAGGA 1980
GGTGGACTTC TCACAACAGA GGCCCAGCCA GGGAGGACTG TATTGTGAGT TCGCTTCCAT 2040
GTCTTCCCTG CTCCTCCACC ACCCTAACCA TTCCTCTCTC AACCATTTTC CATACTGTTC 2100
CTCAGTGATT CACACACCTT TTTCTTCTAA TCCATCAAGA AGTCTCGAGT CCAAGAATAT 2160
TGTCATTTAT TCAAGCATGC ATTTTGTGCT CCATACATTC ATTCAGTTAT TCATTCAACA 2220
AATTTTGTTA GCACTCACTG TGTGCCAGAC GCTATGCATG TAACTGTACT GTGTGCCAGG 2280
CAAGACTAGG CCCTACCCTC AAGGAGTTCA AAGCTAAACA CTCTTTTTTC TCTGTTTTCC 2340
AGGCCCAGAA CAAAACAATG TTCATTACGT ATTTGCTGAA TTACTCACTT TAGCCAACAT 2400
CTATTGTAAA TTTCGTGTAT GTATAACCTA TATTCAGAGG 2440