EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-17090 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr14:35852850-35855390 
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
TGAGGAGGGA GATAGGGGAC CTGCAGGCTG AGGAGGGGTT GGCCAGCCCC AGTGGGACAA 60
GATGGCTGGT GGATGGGGTT CAGAGGACTT TCAGGCAGAA GCACCCCAAA AGTAAGTTTG 120
TGTCTGCTGT GGGAAAGACT GTGGCAAGCA GGTGTGGCAG ATGCATGAAA GGCCTGGGCA 180
CCCTGGAAGG ACATCAGGCT TCATGCTGAG GGAGATGGGA AGCTTGTTGT GGGACAGTAT 240
GAAGGGTAAA CTGAGGGAGG GAGGGGCCTA CAGAGCCAGG ACCTTCCTCA AGAGCCCTGG 300
AAGCTTGGAG GCCAACACAC CCAGCTGCCG TCTGCAGCGG CATTGGATGC AGCACAAATG 360
GGGGAGAAGC CCTGGGGAGC AGTTTCAGGA GAGGAAGAGG GTGGGGAAAG GGCTCAGCAA 420
GTTGGGGAAC CAGTGGAATG GTGACAAGGC CAGGTGGAGG CTGGCTGTAT TTTGGGGGCA 480
TCCAGTGCCC CATCCTAAGA GCACCCTGAC CTCCTTGGAG GAGATCGCCT TATGCCCGCT 540
TCCCTCAAGG AGGGCCAAAG GGGTCATATC CTTCCCAGCC AGCCCCAACC TGGGACAGGA 600
ATGTGGCGTC CCCTGGCCAA TTGGTTGTTC TTGCCTAGGG CTTTGGCTCC TGAGTGAGTG 660
AGATGAGGAC ACTGGTGGTA AGAGGTCCTT TATAAAAGCA GGTGCGGCAG CAGTGGCTGT 720
GGCCCCGGGG TCCTGGCCGA GACTGGCTGA CTGGCTTCCG TCCCCAGAGC CCTCACTTCC 780
TGATTTTCCC AAGCCTGGTT TCCCCCTGTC TATTGTCCAT TCTGTGAGCT CTCCCCACTG 840
TGGACTTCCA TTAAATTCCC CGCTGCTTAA ACTAGCCAGA GTCAGTTTCC TGCTCCCAGA 900
CACAAGCATG GGCCTGAGTC AGCCGCTCAA CTGACGTCCG TGGAGTCAGC TGGAGTCTCT 960
GCAGTTTGCT CCTCACAGTG CATCTTGAAC CTGATTCATT CCCCTGACCT CTCTCCAGAT 1020
CTGCATTTTC TCACTCCTGG GCAGCTGCAG CTGCTTCCAG CCTGGGCTTC CTCCCAGCTC 1080
TCTACATCCT AAGTTCTCTT AAGTATCACT GCTGGACTTT GGTCCTGCAG ACACCCCTGC 1140
TCAAGAAGTT CATGTGGCTC CCGCCGCCCA GTGGTCAAGT CCAGCGTCCA TAGCCTTCTG 1200
TAGCCCGGCC CTGCCCCCTG CCCCGTGACT GGAGAAGCCC TGTGTTCTTG AGGGGCTCCA 1260
GGCGGGTCAC CTTGCAGCCT TCTCCCAATG GAAAGCCTGT CCTAACCTTA GTGAGAGTTC 1320
AGGGTTGGGG GTTGGCTCTC TGGATCTGCG TCAGTGCTCC AAGCAACTGC CTTAGTGGGG 1380
CAGTCACTGA CCCCCCTGGA GTTGCTGCCA TCTACAGAAG GCCTGGGCTG GGTCAGGTGG 1440
CCGCTGGCCG TTCCTCACAG CGGAACGGAT GCTCTGCAAA GGCCCTCCTG ACTTTTGTTC 1500
ACTTCGTCCC TTTGTGAGGC CCCAGCCCTG GCAGAGGTCA TGGAGGGACC ATCCAAAGGC 1560
CCCGCCTTCT CCACCTTCAT CATTGCAATC CCATGAGCCA GGTGGGCACA GGTGGCTTGC 1620
ACTGTGGAAC CTCAGGAAAA AGGAGACAGG CATTGATGCC AGCCCCACAG AGGCACAGAG 1680
CTCTTCCTTG GCGCCTGCTG TGTGGACAAA GGCCTGGCCA GTGTGCGGAG TCTGGGGTTC 1740
TGTGATGCCA CAGGCCCTGC CTCTGTGTGA GCTGCTGCCT GCAGGGCCTC CCTCACCCTG 1800
CAGCCTCATC ACCTCCTGAC CATTGCAGGC AACCGACCAA GCTCTCGTGT GAGGTGGGCA 1860
CCCCCTGGGC TGTCTCTCCA GCTTACAAGA ATGGCCCCCT TTCAAGTCAT TGCCTTGAGC 1920
TGTCTAGACC CATCCAGGCA GGGTTTTAGC ACAAGGCTCT CAGGAGTTAA ACATGCCATG 1980
AAACATGCCC CACTTCCCAG GATATAATTA GACCAGAGTC CTCTCCCTGG GAGTGTGTGC 2040
GTGTCAGAGA GAGACAAAGA GAAAGAGAGG GAGGGAGGAA GGGAGGGAGG GAGGCGGAGA 2100
TTGGCTGAGG GCCTGTCTCT GGTTCGGGGC CTGTCACCCA TGAGCAGCTT GGCTCCCCGC 2160
TGAGTTCCCT CGCCTCTTGC CATTGGCAAG ACACACGGAG GAAGGCTCCT GCAGAGAAGA 2220
CAGACAGGCA AAGCTCCTCA GAGGGGAGCT GGCCAGGAGG CCCAGGCCTC ACCCACCCCG 2280
TCACTGTCCT GGCTCTGAGG CCATCCTCAC CCCTTGCTGC AGGGGCTTAC CCATCTCCAC 2340
TGGGTTAGGC TGTGTGCCCG ACTGGCCTTT TTCCTCTGGG TATTTGGGGC ATGCTCACCT 2400
GTGGACTAAT GTTTTTGAGA ACAAATTTTA AATGTTAATA GCCTTATTTT TTTTTTCTGA 2460
TAAAGTAATA GAGGAAAACA TTAAAAAGAG AGTAAATCTC CCTGCTTTGT TTTGCTTTGA 2520
GGGTCTGGCT CTGTTGCCCA 2540