EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-23814 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr14:35852840-35855660 
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: 4             
ChromosomeStartEnd
chr143585350935853868
chr143585335235855322
chr143585295435853087
chr143585312335853347
Number: 1             
IDChromosomeStartEnd
GH14I035383chr143585251035856380
Enhancer Sequence
CTTAGAAACC TGAGGAGGGA GATAGGGGAC CTGCAGGCTG AGGAGGGGTT GGCCAGCCCC 60
AGTGGGACAA GATGGCTGGT GGATGGGGTT CAGAGGACTT TCAGGCAGAA GCACCCCAAA 120
AGTAAGTTTG TGTCTGCTGT GGGAAAGACT GTGGCAAGCA GGTGTGGCAG ATGCATGAAA 180
GGCCTGGGCA CCCTGGAAGG ACATCAGGCT TCATGCTGAG GGAGATGGGA AGCTTGTTGT 240
GGGACAGTAT GAAGGGTAAA CTGAGGGAGG GAGGGGCCTA CAGAGCCAGG ACCTTCCTCA 300
AGAGCCCTGG AAGCTTGGAG GCCAACACAC CCAGCTGCCG TCTGCAGCGG CATTGGATGC 360
AGCACAAATG GGGGAGAAGC CCTGGGGAGC AGTTTCAGGA GAGGAAGAGG GTGGGGAAAG 420
GGCTCAGCAA GTTGGGGAAC CAGTGGAATG GTGACAAGGC CAGGTGGAGG CTGGCTGTAT 480
TTTGGGGGCA TCCAGTGCCC CATCCTAAGA GCACCCTGAC CTCCTTGGAG GAGATCGCCT 540
TATGCCCGCT TCCCTCAAGG AGGGCCAAAG GGGTCATATC CTTCCCAGCC AGCCCCAACC 600
TGGGACAGGA ATGTGGCGTC CCCTGGCCAA TTGGTTGTTC TTGCCTAGGG CTTTGGCTCC 660
TGAGTGAGTG AGATGAGGAC ACTGGTGGTA AGAGGTCCTT TATAAAAGCA GGTGCGGCAG 720
CAGTGGCTGT GGCCCCGGGG TCCTGGCCGA GACTGGCTGA CTGGCTTCCG TCCCCAGAGC 780
CCTCACTTCC TGATTTTCCC AAGCCTGGTT TCCCCCTGTC TATTGTCCAT TCTGTGAGCT 840
CTCCCCACTG TGGACTTCCA TTAAATTCCC CGCTGCTTAA ACTAGCCAGA GTCAGTTTCC 900
TGCTCCCAGA CACAAGCATG GGCCTGAGTC AGCCGCTCAA CTGACGTCCG TGGAGTCAGC 960
TGGAGTCTCT GCAGTTTGCT CCTCACAGTG CATCTTGAAC CTGATTCATT CCCCTGACCT 1020
CTCTCCAGAT CTGCATTTTC TCACTCCTGG GCAGCTGCAG CTGCTTCCAG CCTGGGCTTC 1080
CTCCCAGCTC TCTACATCCT AAGTTCTCTT AAGTATCACT GCTGGACTTT GGTCCTGCAG 1140
ACACCCCTGC TCAAGAAGTT CATGTGGCTC CCGCCGCCCA GTGGTCAAGT CCAGCGTCCA 1200
TAGCCTTCTG TAGCCCGGCC CTGCCCCCTG CCCCGTGACT GGAGAAGCCC TGTGTTCTTG 1260
AGGGGCTCCA GGCGGGTCAC CTTGCAGCCT TCTCCCAATG GAAAGCCTGT CCTAACCTTA 1320
GTGAGAGTTC AGGGTTGGGG GTTGGCTCTC TGGATCTGCG TCAGTGCTCC AAGCAACTGC 1380
CTTAGTGGGG CAGTCACTGA CCCCCCTGGA GTTGCTGCCA TCTACAGAAG GCCTGGGCTG 1440
GGTCAGGTGG CCGCTGGCCG TTCCTCACAG CGGAACGGAT GCTCTGCAAA GGCCCTCCTG 1500
ACTTTTGTTC ACTTCGTCCC TTTGTGAGGC CCCAGCCCTG GCAGAGGTCA TGGAGGGACC 1560
ATCCAAAGGC CCCGCCTTCT CCACCTTCAT CATTGCAATC CCATGAGCCA GGTGGGCACA 1620
GGTGGCTTGC ACTGTGGAAC CTCAGGAAAA AGGAGACAGG CATTGATGCC AGCCCCACAG 1680
AGGCACAGAG CTCTTCCTTG GCGCCTGCTG TGTGGACAAA GGCCTGGCCA GTGTGCGGAG 1740
TCTGGGGTTC TGTGATGCCA CAGGCCCTGC CTCTGTGTGA GCTGCTGCCT GCAGGGCCTC 1800
CCTCACCCTG CAGCCTCATC ACCTCCTGAC CATTGCAGGC AACCGACCAA GCTCTCGTGT 1860
GAGGTGGGCA CCCCCTGGGC TGTCTCTCCA GCTTACAAGA ATGGCCCCCT TTCAAGTCAT 1920
TGCCTTGAGC TGTCTAGACC CATCCAGGCA GGGTTTTAGC ACAAGGCTCT CAGGAGTTAA 1980
ACATGCCATG AAACATGCCC CACTTCCCAG GATATAATTA GACCAGAGTC CTCTCCCTGG 2040
GAGTGTGTGC GTGTCAGAGA GAGACAAAGA GAAAGAGAGG GAGGGAGGAA GGGAGGGAGG 2100
GAGGCGGAGA TTGGCTGAGG GCCTGTCTCT GGTTCGGGGC CTGTCACCCA TGAGCAGCTT 2160
GGCTCCCCGC TGAGTTCCCT CGCCTCTTGC CATTGGCAAG ACACACGGAG GAAGGCTCCT 2220
GCAGAGAAGA CAGACAGGCA AAGCTCCTCA GAGGGGAGCT GGCCAGGAGG CCCAGGCCTC 2280
ACCCACCCCG TCACTGTCCT GGCTCTGAGG CCATCCTCAC CCCTTGCTGC AGGGGCTTAC 2340
CCATCTCCAC TGGGTTAGGC TGTGTGCCCG ACTGGCCTTT TTCCTCTGGG TATTTGGGGC 2400
ATGCTCACCT GTGGACTAAT GTTTTTGAGA ACAAATTTTA AATGTTAATA GCCTTATTTT 2460
TTTTTTCTGA TAAAGTAATA GAGGAAAACA TTAAAAAGAG AGTAAATCTC CCTGCTTTGT 2520
TTTGCTTTGA GGGTCTGGCT CTGTTGCCCA GGCTGGAGTG CAGTGGCGCG ATCTCAGCTC 2580
ACTGCAGCCT TGACCTCCTG GGCTCAAGGG ATGCTCTCAC CTCAGCCTCT GGGACTAAAG 2640
GCATGTGCCA CGACACTCAG CTAATTTTGT TTAGTTTTCG TAGAGACGAG GTCTCACTAT 2700
GTTATCCAGG CTGGTCTCAA ACTCCTGGGC TCAAGCAATC CTCCCACCTT GGCCTCCCAA 2760
AGTTCTGAGA TTACAGGCAG GAGCCAAGGT GACTGGCCTA TTGTTAGTTT TTTAAAGTGT 2820