EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-30103 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr5:133433940-133436930 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr5:133434774-133434792GGAGAGAAGGAAGGCGGG+6.24
NFAT5MA0606.1chr5:133436081-133436091AATGGAAAAT-6.02
NFATC1MA0624.1chr5:133436081-133436091AATGGAAAAT-6.02
NFATC3MA0625.1chr5:133436081-133436091AATGGAAAAT-6.02
NFKB1MA0105.4chr5:133436370-133436383CGGGGAATCCCCT+7.12
NFKB1MA0105.4chr5:133436370-133436383CGGGGAATCCCCT-7.22
Pou2f3MA0627.1chr5:133436058-133436074TTTGATTTGCATACGA-7.19
ZNF263MA0528.1chr5:133435108-133435129TTCCTTTCCACTTCCTCCTCT-6.53
Number of super-enhancer constituents: 22             
IDCoordinateTissue/cell
SE_11859chr5:133434150-133437135CD3
SE_14661chr5:133434420-133437118CD4_Memory_Primary_7pool
SE_15545chr5:133435504-133436989CD4_Memory_Primary_8pool
SE_15868chr5:133435555-133437149CD4_Naive_Primary_7pool
SE_16541chr5:133435396-133436995CD4_Naive_Primary_8pool
SE_16864chr5:133434714-133437989CD4p_CD225int_CD127p_Tmem
SE_17306chr5:133434013-133442187CD4p_CD25-_CD45RAp_Naive
SE_17779chr5:133433894-133442397CD4p_CD25-_CD45ROp_Memory
SE_18300chr5:133434019-133437989CD4p_CD25-_Il17-_PMAstim_Th
SE_19131chr5:133434895-133438108CD4p_CD25-_Il17p_PMAstim_Th17
SE_20200chr5:133434504-133437215CD56
SE_21652chr5:133435194-133437085CD8_Naive_7pool
SE_21973chr5:133435115-133437911CD8_Naive_8pool
SE_22418chr5:133434549-133438019CD8_primiary
SE_30897chr5:133434103-133437128Fetal_Thymus
SE_39383chr5:133435462-133437005Jurkat
SE_49860chr5:133434230-133435393RPMI-8402
SE_49860chr5:133435431-133437058RPMI-8402
SE_50485chr5:133434455-133437093Sigmoid_Colon
SE_55097chr5:133434867-133436879Thymus
SE_62337chr5:133403949-133487040Tonsil
SE_66306chr5:133435462-133437005Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr5133435759133436442
chr5133434800133435400
chr5133436200133436400
chr5133436400133436600
Number: 1             
IDChromosomeStartEnd
GH05I134098chr5133433961133438092
Enhancer Sequence
AGTGGCACGA TGTCAGCTCA TTGCAACCTC CATTACCTCT CAGGTTCAAG CAATTCTCCT 60
GCCTCAGCCT CCCAAATAGC TGGGATTACA GGCACCCACC ACCATGCTGG GATTACAGGC 120
ACCCACCACC ATGACCGGCT AATTTTTGTA TTTTTGGTAG AGACAAGGTT TCACCATATT 180
GGCCAGGCTT GTCTCAAACT CCTGACTTCG GGTGATCTGC CTGCCTCAGC CTCCCAAAGT 240
GCTGGGATTA CAGGCGTGAG CCACCACACC CGGCCAAGGA TTCCTTTCTT TCAGACCAGT 300
CCTCTGCTAA CCTCTGACAA TGCTCCCCTC TCAACCTCCT GGACAGGTGG TGGTGTCCTG 360
GTGGCCCTGA CCACCAGCTC CATCTTTATA ACATGAAGAC CCTTGGCCCC AGGCCTCTAG 420
GCCTTCTGCA TGAGCTGGGC CTGATCTTTT CCTTGGGGCT GTCTGCAGCC TGCACAAGTG 480
AGGGGACTAA GGCCACGGTG ACCAGGGCAA GTCCAGCTCC TACTCTTACC CTGAGGGGCC 540
CTCCCAGAGG GTTGAGTCAC CTGGGGAGGG AGCAAAGTGC AAAAGGTCCA AGTTCTAGTC 600
CACAATGGGT AGGAAAACAA ACCAGCTCAG CTGCACCAGA TCCAAAGTCA TGTTTGAAGG 660
CCTGTAATTT TGAAGGCCGA ACCTGTTCAG GAGCAGTGGG CAAGCCAGGC TGGACTCCAG 720
GCTCTGATCC TGAAGGAGCA ATGAGAAGGG AGACCAGGCG CCGCTGGGGC TGCACAAATA 780
CTGGGTAAAA TTCTGACACA GAGGAGAAAC GGAGACTCAT AGAGAGACAC TGTAGGAGAG 840
AAGGAAGGCG GGCAGAGAGG TGGACAGGCA GGAAAGGCAG GACTCATTGA AACTTACCAG 900
CTCACAGCCT GTGTGCTTCA GGTCGAGCAC AGACTCTTAA AAGTAGGGCT TTGGGTGGAC 960
TGTGATTTAG GCCATCAAAA AAAGCCAGCA TCTGGTTGGG TCTGGCTTGG GGAGGGTGGC 1020
TCCGGCTTAC CCTCTGTCAC TGCAGAACTG CTCTTCAATG GGACCAGCCT TTTACATTCC 1080
CAGAAAGCCC CTCTGCTTCT CAGGGCCCTA AAGGTGCCGT TTGGGGATGC TAGAGGAGGC 1140
TGGAGCCCAT GGGGTCCCTC TCACCCGCTT CCTTTCCACT TCCTCCTCTG GCTCATGCTC 1200
CTTATCTGAC CAGCCTGGCG CAGTCCGGCA CAGCTGCAGA GGGTCAGAGC ATCACGTCTG 1260
GGGAGTCATA ATGAACATGC TGCACGGCCT CCTGGAGGCA GCCTTTCTCA CCTTTCTCAA 1320
CCACCTTCTT TTTTTAACTT TTACTTTTTG AGACAGGATC TTGCTCTGTC ACCCAGGCTA 1380
GAGGGCAGTG GTGCAATCAC AACACGCAGC AGCGTTGACC TCTTTGGCTT AAGCAATTCT 1440
CCCAGCTCAG CCTCCCAAGT AGCTGGACTA CAGGCGCATG CCATCATCCC CAGCTAATTT 1500
TGTTTTTATT TTTTGTAGAG ACAGGGTCTC CCTAAGTTGC CCAGGCCGGT CTCAAACTCC 1560
TGGACTCAAG TAATCCTCCA GTCTCGGCCT CTCAAAGTGC TGGGATTGTG GGTGAGAGCC 1620
ACCATGCCTG GCCCCAACTA CCTTCTTTAT CTCCCCAGAA CCTATCGTCC AGGCCCAGGG 1680
TTGAGACAGA GTGGGAAGGG GTCCATCCCA CATTCCCCAG GCCTCGCTGG TACAGCCTGG 1740
CCCCTTGGTT GGTATGGGGT CAATCCAAAC ACGCCCTGTG AGCCCAGCCT TATGTGGCTG 1800
GCCCTGTGCA TAGGCACAGG CAGAGAAAAC AGAAGCAGCA GGATGCTTTT TATTTGTTAA 1860
TCTAGCTTTG ATGCCCCACC TCCTTCTCAC AAGGAGTGGA GGCCCCTCAG GGAGTACTAA 1920
GTGCCAGGAG TATAGACCCT AGCAGTGGCC TGGGCTGGTC TCCAGGAGGA GGAGGCAGTC 1980
AGGGCTCTCC CTGAAAGCAA GCTGGGGTTA AATATTTTTA GGGCAGAGGA GGCACAAACC 2040
AGCCAGAGCT ACCTTCCTTT CTAATCTTAC CCAGGCATTA AGCTTTGAGA GTATCCCCCT 2100
CATTTACATA CATTCACATT TGATTTGCAT ACGATGCAAA GAATGGAAAA TTCCCCCAGT 2160
GCTTAGCCCC AAGATTACAG TCTCTAATAC TTTATTCCCA CAACCGCGGC ACCCCGTGAC 2220
AGACAGGGGG TCCTGCCTGT GATCTAGATC TGGGCTCCCT GCAGCCTGGG ACCCAGCCTG 2280
CAGCCTCCTG CCTAGAGGTA GCAGCTCCTG TGAAGGGGGT GGCAGCAGCA GACGCAGGCC 2340
TAGCAAAACA AGGTACTTTC ACATGTGACT CACACCAAGG ACCAGAAGCA GAATTACAGT 2400
GTGAAAAACC AGAGCCGGCC GAGACTCCGT CGGGGAATCC CCTCCAGCTC CCTCTCTGTT 2460
TCACTCCTTT AAAAAGCCCT GGCCATGGCC CAGCACTCTA GAACCCTCCA AGAAAGTGCT 2520
GTGCCTCCCA TCCAGGATGG GCAGGGGCCA TGGCACTTCA GCCAGGCCCC TTGACTTTCT 2580
CTCTGGGTTC TTGGGCTCAG AAATTACATC TAAGCAGAGA AAGAGGCAGA AGTGGATTCA 2640
TCCCAGGGGC AGAGCTGGAA CTGGACCTGG GAGCAGTTGC TGCCTTGCAG GCCCCAGGGC 2700
TCCATGCTCA TATTTTTCTT GGCCTGGCTT CCTCCTTCTG ATCCATTCTC TGAGCTACCC 2760
ATACACATGC AGCAAACTAT TCTGCAAGAC CACCAGAGCT GATTTCTGTT GCTTGCAAGG 2820
AGTAATCCCA ACGGAAACCA GACATTCTCT GTGATGGCAG GATGCCCTGA AGTCCTTGAC 2880
GAAGGCCACC TTCAGCTCCT GACACATGTC TGGATTTTCT GCCACCCTCA AGGGACCAGC 2940
ATGGCTTCAA ATCCTGCTCC TCTCAGTTTC CAGGGGCCTG ACCTTGGGCA 2990