EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-15065 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr14:69433020-69435200 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr14:69434639-69434650GAGCCATAAAA+6.14
EWSR1-FLI1MA0149.1chr14:69434314-69434332GTAATGAAGGCAGGCAGG+6.1
GATA2MA0036.3chr14:69434411-69434422GAAGATAAGAA-6.02
TBX20MA0689.1chr14:69433302-69433313TTTCACACCTA-6.14
TBX2MA0688.1chr14:69433302-69433313TTTCACACCTA-6.32
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00359chr14:69432637-69434133Adipose_Nuclei
SE_01544chr14:69430779-69440176Aorta
SE_04266chr14:69434313-69439200Brain_Anterior_Caudate
SE_09473chr14:69432758-69434788CD14
SE_16061chr14:69431886-69439120CD4_Naive_Primary_7pool
SE_17458chr14:69430603-69440146CD4p_CD25-_CD45RAp_Naive
SE_21813chr14:69432767-69438945CD8_Naive_7pool
SE_22077chr14:69431757-69439364CD8_Naive_8pool
SE_24115chr14:69433642-69434209Colon_Crypt_2
SE_25810chr14:69432769-69434737Duodenum_Smooth_Muscle
SE_26589chr14:69431463-69435323Esophagus
SE_28065chr14:69430429-69433825Fetal_Intestine
SE_28974chr14:69430152-69434386Fetal_Intestine_Large
SE_31722chr14:69433220-69434168Gastric
SE_36138chr14:69431687-69434613HMEC
SE_37016chr14:69421047-69434233HSMMtube
SE_38329chr14:69434966-69438171HUVEC
SE_42569chr14:69433133-69435119Lung
SE_45678chr14:69432799-69434803Osteoblasts
SE_48719chr14:69432770-69437674Right_Atrium
SE_50146chr14:69430716-69447464Sigmoid_Colon
SE_52675chr14:69432830-69437821Small_Intestine
SE_53596chr14:69433132-69434043Spleen
SE_54485chr14:69427192-69447448Stomach_Smooth_Muscle
SE_55584chr14:69433888-69435904Thymus
SE_58222chr14:69431261-69434234VACO_9m
SE_58222chr14:69434269-69434674VACO_9m
SE_65495chr14:69433280-69434266Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146943485769435075
Number: 1             
IDChromosomeStartEnd
GH14I068961chr146942810969440104
Enhancer Sequence
TGGCATCACC GCAGACCCCA GAGATCATCT GCATGTGATA ATCCAAGTAC AGCCTTTAGA 60
ACAGAGCCCC ACCACCATCC TACCATCCAA TTTCTCGGTT TATAGGTGGT TTCAGGTGTG 120
ACTTATCCAG CATCACAAAG TGGCCACAGG CAGCACTAGG ACAAGACCTC GGGTCTCCTG 180
AGGCCCCGGT ACCTAACACA CAACCATTCT TCCTGTTCCT GGGGGACAAG ATAGGTTTCT 240
GCCAAACAAC TCTCTGGCCT AATAAATCAA AGAAGACAGT CTTTTCACAC CTATCCCCAC 300
TCCCAAATGC CACTCCCAAA GTCCCAACAG AAAGGGAGCA GGAGGCAGGT GAAAGCTTTG 360
CTGAGGCCCC ACAGTTATCT AGATCCACAC CCCTCGGGAT ACTGTGGCTA AAGACAGTGG 420
GCTGCTGACG TCCAACACTC CAGAGAGAAC CCTCAGCAGA GGGACTGGAA GGAGAAGGAA 480
AACCAAGACC CAGGTTTTAC TTCCTTTAAG GTCCACAAAC CCACACAAAA GGACCAGAAA 540
TTCCCTGTGA TTTTCTGAAG CAGGGCTCAG CCAAATGCAA TAACCCCACC CTCCAGAGAG 600
GAAGGGGCAG GATGAAGAGG GACATGTCAG TATGGCCAGC ACCTTGGAAT CTGATGGGCT 660
GTTAGCCAAA GAAAAAACGC AGCTAGGCTG GCTGGTAGGG AGCTGGGAGG TCTGTGCCAG 720
TTCCAACCAG CCTACCATTG GACGCACCAG CTCAGAGAGG GGCGCTGAGC AGCATGGCAG 780
GGGCTGAGGT CATCCTAGGC TATGACCCCA TCCCAATGAC AAGGCCAGCT TCCCTGGCCC 840
CTGTCCTCCT TCTGATTCCA GGACACACCT CTTAGTCCTG AGGAGCCAAC TGGGCCTCTG 900
CCCTGGTCCC AGCAATCAAC CTCATCTCTG GGGTGGTCCT TGGTGACTCA GACTACCACC 960
ACCCAGGCCC TCAGCATCTG TCAGTTGTCT CCTGCAGGAC TACAGCTGCC ACACTCCTGT 1020
CCAAAGGCCC TCACCACCAC TGTTCATCAA CACTGGATAC TCGGTGAATA CCTAGTATGT 1080
GCAAGCTTGA TTCGTGCTTA CCTGCTCTTT GGGGTGCTGG GATGAGCTCA TCAGGGAGCT 1140
CCTGAAAGTC CATTACTAGG GGGACCCCAG GAGACTCCAC AAATCCACCT TTGATCATCC 1200
AAGGAGCCTC AGATCAGTTA CAGATCAGTG ACATCCCCTG AGAATCCTCT AAATGTCTTT 1260
AGAGAGGAGT TTCACAACAG TGCCCCAAGA AAGTGTAATG AAGGCAGGCA GGCTGCCACA 1320
TATCTGTCCT TTCTGACTCT CCTAGCCCAG GTACTAACTG GGCAAGGCAA TGGCCGAGTG 1380
GCTGAGAGCC AGAAGATAAG AAGGCAAGAG GAGGGAAATC AGACAGGGAC AAAGGCCACT 1440
CAACTGGGAC CCCACTTGTT GTCCTTGAAG CCTAGGAATG GTCCTGGCGG AGTGGGGCTC 1500
ATCGTGGCTC CCCACATCTG GCCTCTTCCA AAACTCTACA TGCAGCCCAA GCCTCATATC 1560
CAGAGCAGTC TCTTGTCTTG CAGAGCACAG CCAGCTTCCA AATGGCACAA GAGGCTGCTG 1620
AGCCATAAAA TATAAACTCA TTTAGAAGCA TTCCCAAATT CACGCACCTT TTCGTCATGA 1680
CACATTTGCT TTATCAAGAA GTAATAAAAG CACAACTACT ACCCTGGGAG GTGAAAAAAA 1740
TGGCAACGTG GCATAGGTCC CTAGGAACCT GAATCTCAAG CCCAGGAAAA GAGGGCAGCA 1800
GGCAAGGGAC CAGGGACCCA TAGGTACGGA CACCAGATGC CACACACACG TGTGGGTGGA 1860
AAGAGAGTAA GATACTGAGA CTGACGTCTC CTGCCCTCCC TCATCAAACA TCAGCAAGTC 1920
TTTGAACACT GGCGGGGTGC AGGGTGGCAG GTGTAACATA CGAACGCCAC CGCAGAGGCA 1980
GGAAGCCGGG TTCAGTCCCA CCTGCCACCT ACAAGTTGCT GTGTGACCTG GGCAAGTGCT 2040
TTGGAACTCA GCAGTCTCAG CCACAAAACA GGGATGGCAG AGCTCCCACA GGTCTACCTT 2100
TACAGCTCCA GGGCAAAGGA GATGTGGGAG CAAAAGGAGC AATGAACAGA GTGATGCATT 2160
GGGTATGACC CCATCTACAC 2180