EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-11220 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr14:35852670-35855460 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:35854914-35854932GAGAGGGAGGGAGGAAGG+6.27
EWSR1-FLI1MA0149.1chr14:35854918-35854936GGGAGGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr14:35854922-35854940GGGAGGAAGGGAGGGAGG+6.92
EWSR1-FLI1MA0149.1chr14:35854926-35854944GGAAGGGAGGGAGGGAGG+7.08
HNF4GMA0484.1chr14:35853962-35853977TGGACTTTGGTCCTG-6.24
SOX10MA0442.2chr14:35855352-35855363TGCTTTGTTTT-6.02
ZNF263MA0528.1chr14:35853239-35853260AGAGGAAGAGGGTGGGGAAAG+6.32
ZNF263MA0528.1chr14:35854916-35854937GAGGGAGGGAGGAAGGGAGGG+7.5
ZNF263MA0528.1chr14:35854923-35854944GGAGGAAGGGAGGGAGGGAGG+7.9
ZNF263MA0528.1chr14:35854920-35854941GAGGGAGGAAGGGAGGGAGGG+8.23
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_00565chr14:35852740-35855391Adipose_Nuclei
SE_06617chr14:35852268-35856149Brain_Hippocampus_Middle
SE_23298chr14:35852780-35855350Colon_Crypt_1
SE_26422chr14:35852301-35855862Duodenum_Smooth_Muscle
SE_26613chr14:35852665-35856450Esophagus
SE_27693chr14:35852756-35855637Fetal_Intestine
SE_28626chr14:35852541-35855532Fetal_Intestine_Large
SE_30638chr14:35852799-35856205Fetal_Muscle
SE_31925chr14:35852742-35855477Gastric
SE_34831chr14:35853005-35855686HeLa
SE_41052chr14:35852684-35856919Left_Ventricle
SE_42211chr14:35852557-35856488Lung
SE_48930chr14:35852885-35856463Right_Atrium
SE_50091chr14:35852611-35855733Sigmoid_Colon
SE_52425chr14:35852462-35855524Small_Intestine
SE_53368chr14:35852609-35855549Spleen
SE_55029chr14:35851981-35857162Stomach_Smooth_Muscle
SE_56156chr14:35852273-35855766u87
SE_65723chr14:35852678-35855600Pancreatic_islets
SE_67556chr14:35852273-35855766u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr143585350935853868
chr143585335235855322
chr143585275435852892
chr143585295435853087
chr143585312335853347
Number: 1             
IDChromosomeStartEnd
GH14I035383chr143585251035856380
Enhancer Sequence
CAGGAAAAGT GCTACCTGCA AAAATGGGAG GGGAAAGGAA TGGAACCAGG AGTGGTCATT 60
AAAAGGGAAA AAGGATTGCA AGCAAATGGC ACAAAATGTG ATATTTCTGG GGGGAATAAA 120
TGCATTGGTT GAGATATGTA CAAACGTGGT GGGATCAAGG AGAAGGAGCA CTTAGAAACC 180
TGAGGAGGGA GATAGGGGAC CTGCAGGCTG AGGAGGGGTT GGCCAGCCCC AGTGGGACAA 240
GATGGCTGGT GGATGGGGTT CAGAGGACTT TCAGGCAGAA GCACCCCAAA AGTAAGTTTG 300
TGTCTGCTGT GGGAAAGACT GTGGCAAGCA GGTGTGGCAG ATGCATGAAA GGCCTGGGCA 360
CCCTGGAAGG ACATCAGGCT TCATGCTGAG GGAGATGGGA AGCTTGTTGT GGGACAGTAT 420
GAAGGGTAAA CTGAGGGAGG GAGGGGCCTA CAGAGCCAGG ACCTTCCTCA AGAGCCCTGG 480
AAGCTTGGAG GCCAACACAC CCAGCTGCCG TCTGCAGCGG CATTGGATGC AGCACAAATG 540
GGGGAGAAGC CCTGGGGAGC AGTTTCAGGA GAGGAAGAGG GTGGGGAAAG GGCTCAGCAA 600
GTTGGGGAAC CAGTGGAATG GTGACAAGGC CAGGTGGAGG CTGGCTGTAT TTTGGGGGCA 660
TCCAGTGCCC CATCCTAAGA GCACCCTGAC CTCCTTGGAG GAGATCGCCT TATGCCCGCT 720
TCCCTCAAGG AGGGCCAAAG GGGTCATATC CTTCCCAGCC AGCCCCAACC TGGGACAGGA 780
ATGTGGCGTC CCCTGGCCAA TTGGTTGTTC TTGCCTAGGG CTTTGGCTCC TGAGTGAGTG 840
AGATGAGGAC ACTGGTGGTA AGAGGTCCTT TATAAAAGCA GGTGCGGCAG CAGTGGCTGT 900
GGCCCCGGGG TCCTGGCCGA GACTGGCTGA CTGGCTTCCG TCCCCAGAGC CCTCACTTCC 960
TGATTTTCCC AAGCCTGGTT TCCCCCTGTC TATTGTCCAT TCTGTGAGCT CTCCCCACTG 1020
TGGACTTCCA TTAAATTCCC CGCTGCTTAA ACTAGCCAGA GTCAGTTTCC TGCTCCCAGA 1080
CACAAGCATG GGCCTGAGTC AGCCGCTCAA CTGACGTCCG TGGAGTCAGC TGGAGTCTCT 1140
GCAGTTTGCT CCTCACAGTG CATCTTGAAC CTGATTCATT CCCCTGACCT CTCTCCAGAT 1200
CTGCATTTTC TCACTCCTGG GCAGCTGCAG CTGCTTCCAG CCTGGGCTTC CTCCCAGCTC 1260
TCTACATCCT AAGTTCTCTT AAGTATCACT GCTGGACTTT GGTCCTGCAG ACACCCCTGC 1320
TCAAGAAGTT CATGTGGCTC CCGCCGCCCA GTGGTCAAGT CCAGCGTCCA TAGCCTTCTG 1380
TAGCCCGGCC CTGCCCCCTG CCCCGTGACT GGAGAAGCCC TGTGTTCTTG AGGGGCTCCA 1440
GGCGGGTCAC CTTGCAGCCT TCTCCCAATG GAAAGCCTGT CCTAACCTTA GTGAGAGTTC 1500
AGGGTTGGGG GTTGGCTCTC TGGATCTGCG TCAGTGCTCC AAGCAACTGC CTTAGTGGGG 1560
CAGTCACTGA CCCCCCTGGA GTTGCTGCCA TCTACAGAAG GCCTGGGCTG GGTCAGGTGG 1620
CCGCTGGCCG TTCCTCACAG CGGAACGGAT GCTCTGCAAA GGCCCTCCTG ACTTTTGTTC 1680
ACTTCGTCCC TTTGTGAGGC CCCAGCCCTG GCAGAGGTCA TGGAGGGACC ATCCAAAGGC 1740
CCCGCCTTCT CCACCTTCAT CATTGCAATC CCATGAGCCA GGTGGGCACA GGTGGCTTGC 1800
ACTGTGGAAC CTCAGGAAAA AGGAGACAGG CATTGATGCC AGCCCCACAG AGGCACAGAG 1860
CTCTTCCTTG GCGCCTGCTG TGTGGACAAA GGCCTGGCCA GTGTGCGGAG TCTGGGGTTC 1920
TGTGATGCCA CAGGCCCTGC CTCTGTGTGA GCTGCTGCCT GCAGGGCCTC CCTCACCCTG 1980
CAGCCTCATC ACCTCCTGAC CATTGCAGGC AACCGACCAA GCTCTCGTGT GAGGTGGGCA 2040
CCCCCTGGGC TGTCTCTCCA GCTTACAAGA ATGGCCCCCT TTCAAGTCAT TGCCTTGAGC 2100
TGTCTAGACC CATCCAGGCA GGGTTTTAGC ACAAGGCTCT CAGGAGTTAA ACATGCCATG 2160
AAACATGCCC CACTTCCCAG GATATAATTA GACCAGAGTC CTCTCCCTGG GAGTGTGTGC 2220
GTGTCAGAGA GAGACAAAGA GAAAGAGAGG GAGGGAGGAA GGGAGGGAGG GAGGCGGAGA 2280
TTGGCTGAGG GCCTGTCTCT GGTTCGGGGC CTGTCACCCA TGAGCAGCTT GGCTCCCCGC 2340
TGAGTTCCCT CGCCTCTTGC CATTGGCAAG ACACACGGAG GAAGGCTCCT GCAGAGAAGA 2400
CAGACAGGCA AAGCTCCTCA GAGGGGAGCT GGCCAGGAGG CCCAGGCCTC ACCCACCCCG 2460
TCACTGTCCT GGCTCTGAGG CCATCCTCAC CCCTTGCTGC AGGGGCTTAC CCATCTCCAC 2520
TGGGTTAGGC TGTGTGCCCG ACTGGCCTTT TTCCTCTGGG TATTTGGGGC ATGCTCACCT 2580
GTGGACTAAT GTTTTTGAGA ACAAATTTTA AATGTTAATA GCCTTATTTT TTTTTTCTGA 2640
TAAAGTAATA GAGGAAAACA TTAAAAAGAG AGTAAATCTC CCTGCTTTGT TTTGCTTTGA 2700
GGGTCTGGCT CTGTTGCCCA GGCTGGAGTG CAGTGGCGCG ATCTCAGCTC ACTGCAGCCT 2760
TGACCTCCTG GGCTCAAGGG ATGCTCTCAC 2790