EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-05318 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr10:5650950-5653510 
TF binding sites/motifs
Number: 25             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:5652508-5652526GGAAGGAAGGAGAGAGAG+6.03
EWSR1-FLI1MA0149.1chr10:5652573-5652591GAAAGGAAAGAAAGAAAG+6.03
EWSR1-FLI1MA0149.1chr10:5652496-5652514AGAATGAAAGAAGGAAGG+6.47
EWSR1-FLI1MA0149.1chr10:5652438-5652456AGAAAGAAGGAGGGAAGG+6.55
EWSR1-FLI1MA0149.1chr10:5652368-5652386GGAGGGAAGGAGGCAAGG+6.84
EWSR1-FLI1MA0149.1chr10:5652446-5652464GGAGGGAAGGAAGGGAAG+7.26
EWSR1-FLI1MA0149.1chr10:5652504-5652522AGAAGGAAGGAAGGAGAG+7.37
EWSR1-FLI1MA0149.1chr10:5652372-5652390GGAAGGAGGCAAGGCAGG+7.61
EWSR1-FLI1MA0149.1chr10:5652500-5652518TGAAAGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr10:5652442-5652460AGAAGGAGGGAAGGAAGG+8.15
HNF4GMA0484.1chr10:5652764-5652779CAGGGACAAAGTCCA+6.19
Hnf4aMA0114.3chr10:5652765-5652781AGGGACAAAGTCCAAC+6.86
IRF1MA0050.2chr10:5652532-5652553AAAAAGAAAGAGAAAAGAAAG-6.07
IRF1MA0050.2chr10:5652609-5652630AGAAAGAAAAAGAAAGAAAGA-6.14
IRF1MA0050.2chr10:5652406-5652427AAAAAAAAAAAGAAAGAAAGG-6.1
IRF1MA0050.2chr10:5652526-5652547AGAAAGAAAAAGAAAGAGAAA-6.27
IRF1MA0050.2chr10:5652647-5652668AGAAAGAAAGAGAAAGAAAGA-6.76
STAT3MA0144.2chr10:5652311-5652322CTTCTGGGAAG+6.14
ZNF263MA0528.1chr10:5652513-5652534GAAGGAGAGAGAGAGAAAGAA+6.01
ZNF263MA0528.1chr10:5652505-5652526GAAGGAAGGAAGGAGAGAGAG+6.04
ZNF263MA0528.1chr10:5652451-5652472GAAGGAAGGGAAGGGAAGGGA+6.29
ZNF263MA0528.1chr10:5652509-5652530GAAGGAAGGAGAGAGAGAGAA+6.66
ZNF263MA0528.1chr10:5652567-5652588GAAGGAGAAAGGAAAGAAAGA+6.73
ZNF263MA0528.1chr10:5652443-5652464GAAGGAGGGAAGGAAGGGAAG+7.36
ZfxMA0146.2chr10:5653277-5653291CCAGCCCAGGCCTG+6.19
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_01811chr10:5649590-5652489Aorta
SE_01811chr10:5652663-5653616Aorta
SE_23669chr10:5651001-5653568Colon_Crypt_1
SE_24448chr10:5651181-5652494Colon_Crypt_2
SE_24448chr10:5652553-5653504Colon_Crypt_2
SE_26546chr10:5650979-5652526Esophagus
SE_26546chr10:5652535-5653597Esophagus
SE_33798chr10:5651350-5653521HCC1954
SE_35816chr10:5650375-5654335HMEC
SE_55779chr10:5650994-5654889u87
SE_58135chr10:5651699-5652394VACO_9m
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1056516975651795
chr1056526505653298
Number: 1             
IDChromosomeStartEnd
GH10I005608chr1056509345653567
Enhancer Sequence
TTTCTGGGAA CGAGAGCCTG AGAAATTCCT TCTCTGCTCA AGGCAGCAGG GGCAGAGGAG 60
ACAGGATTCC CATGCTTCAC TCTCAAACCC CGGCCAGCCG TGCGGGCAGA TGTCACCAGT 120
GCCTGCTGCT GGCAATACCA CTTGGCTCCT TAAATGGTAA ATTCTGCTAA GAAGGTCTCC 180
CTTTTCCAGG AGATATTTTA AAACAAATGC AGTGGACATT TCCCTTCAAA ATGAGATGCA 240
TTCTGTCAAG CAGCTGGCAT TCATTAGGAA ACTAGAGACA AAAAGTATCA CAATCAAATG 300
ACACCATTTG ACAGAGGAGG AAACTGAGCC CCAGAAGTCC AGTGGCAGAG CTGGACCTCC 360
ACTCAGCTCT CCTGGGTCCC CCACAAGGGC CAAGGTGACC GGCTCCCTCT GCCATCCCAG 420
CACCATTATC ACATGCACCA CCCATCCCAT CACTCTGGAA AGGGCCTGAT CTGGACAACG 480
AATTACTTGT CCATTCTGAC TCTAACCCAC TACCTCCAGG ACTTAAGGAA CTAGGAAAGC 540
AAAGAATGGA AAACCAGCAA GTCCTCTTCT TTGGGGGCTT TGTTCTATGT CTGGGGGATG 600
TGAAGCCATC TCCCTCCTAG ATATGAACGA AGACACATGT GGCCTGGAAG GTGTTGGCAG 660
CCACTTTATC ACCATGAGGG AAGCAGTTTG AGGACTCACC TGACCTACAG GGAGAATCAC 720
AGATAACTCC ACCTGCATCT TCCTAAGAGT GAGAACCTTG GAGAAAGTCA ATTCAAACAC 780
TTGCCTTCCC TCAGGAGTCA GTTCTGAGAG CTACCAAGGA GAGGGCAGGA TCAGGGTGAA 840
AAATGACTTG GGTCTCAGAC CCAGAACATT CTACTGGCTG CCTCCAGGAC TCAGTGGGGG 900
GCTAGGAAGG GTTCTCCATC TTCCAAGGGT GTGGAGTGTG CTGTGGGTCA CTCAGAACCT 960
CCCTCTCCTC TTCTGTGATC AGCGGATCTT GTCCAGCCCC TCTCCACTGC TGGCTCACTC 1020
AGCGCCCTCC CCCACCCAGA AACTGCTGGG CTCACCTACT GAGCTATGTG ATCCCTAAGA 1080
AGCTGTCAGA GCTGTACAAG TCTCACAATT CCTTACTCAC TAAGCACTGG CAAGCGCAAG 1140
CTCCAGGGCG TGGCTGTCAG CACTCTGCAC CTTCCTGGAA CTGTCGGGGG AGCATACGGT 1200
CAGCAGCACC ATGCACATCC TTATTGTGCA GCTCAGGAGT CCAAAGCCAA GAACAAGACG 1260
GTGAAGACAG CCCAAGAAGG CTTTTCGGTG CAGTCAATGT CTGACATTTA TGATGCACCC 1320
ACTCACCGGG GACACCGAGT CACATCTGAG CCTCATTTTT TCTTCTGGGA AGACATGCAC 1380
ACTGCCCGAC TCATATCATT CACCTTTGGA CAGGCAAAGG AGGGAAGGAG GCAAGGCAGG 1440
TGCTTCTTTC TAAAAAAAAA AAAAAAAGAA AGAAAGGATA ATAAAGAGAG AAAGAAGGAG 1500
GGAAGGAAGG GAAGGGAAGG GAATAAAGGA GAAGAAGGAA AGAAAAAGAA TGAAAGAAGG 1560
AAGGAAGGAG AGAGAGAGAA AGAAAAAGAA AGAGAAAAGA AAGAAAACAA AAGAAAGGAA 1620
GGAGAAAGGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAAA GAAAGAAAGA 1680
AAGAAAGAAA GAGAGAGAGA AAGAAAGAGA AAGAAAGAAA GAAATCAAGC AAGCAAGCAC 1740
GCACGCACGC ACGGCCCAGG AAGAGAAAAC CAGTGAGTCC TCTCTAAATG GTGAATCAGA 1800
GTCCGTGGCA TAGCCAGGGA CAAAGTCCAA CTTGCCTCTG CCCGGATCTC CGTCTGCTGC 1860
CATCTCCGGA GGCCACACGG CCTGCCCCTC CCCTGCTCGC TCCTCATTCT CTGATGACAG 1920
GTGGTATGAG TGGCTACTCA CCACTCTGAC AGCCTCTCAG CAGCAGACTG TACCCTGGGT 1980
TTGCAGGTAG AGCCTGAGTT ACACCTCCTG AATGCATTAC ACATCACAAC ACTGTCACCA 2040
CACTCTCTTT TGACCTAAAG AAACCCTGCA CTGGGTGACC TCCAAGAAGC CATCTGCCTC 2100
TGATGCTTCT AGGTTAGGCA GCAGGGCTGG GAGAGTGGTA ATATAAACCC CTTCTTTCCA 2160
CTGGGGCCTT TTGGTTTCAG TCCTTGGAAA TATTATTTGT AAAAGAACTT AAAATGCACT 2220
CGCTTTGGGG AAATGCTCAG ATTCAGGAGA CCCCCCGATG GGACATGGAG AGAAGCCGGG 2280
GTCCTGGGGA GGCACCACCT GCCTTGCCTC TTTCTGCACC CCAGCACCCA GCCCAGGCCT 2340
GGCACACAGC AGGGAGGGCT GGCTGGATGC TTCCTAAGCG AGTGGTTATT CTCTAAGTGG 2400
ATACAACCAA TGTGCCGGCC AAACAGATGC ACTGGAGCCT CTAGGTGCTT AGGTTTGGTT 2460
CACGGTCTCG CAGGCATCCA TTGATTGGAA TATATGTAGA CTTACTTTTT TTTTTTTCTT 2520
TTTTTGAGAG GGAGCCTCTC TCTGTCATGA GGCTGGAGTG 2560