EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS146-04482 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr14:35852760-35855670 
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
ACAAAATGTG ATATTTCTGG GGGGAATAAA TGCATTGGTT GAGATATGTA CAAACGTGGT 60
GGGATCAAGG AGAAGGAGCA CTTAGAAACC TGAGGAGGGA GATAGGGGAC CTGCAGGCTG 120
AGGAGGGGTT GGCCAGCCCC AGTGGGACAA GATGGCTGGT GGATGGGGTT CAGAGGACTT 180
TCAGGCAGAA GCACCCCAAA AGTAAGTTTG TGTCTGCTGT GGGAAAGACT GTGGCAAGCA 240
GGTGTGGCAG ATGCATGAAA GGCCTGGGCA CCCTGGAAGG ACATCAGGCT TCATGCTGAG 300
GGAGATGGGA AGCTTGTTGT GGGACAGTAT GAAGGGTAAA CTGAGGGAGG GAGGGGCCTA 360
CAGAGCCAGG ACCTTCCTCA AGAGCCCTGG AAGCTTGGAG GCCAACACAC CCAGCTGCCG 420
TCTGCAGCGG CATTGGATGC AGCACAAATG GGGGAGAAGC CCTGGGGAGC AGTTTCAGGA 480
GAGGAAGAGG GTGGGGAAAG GGCTCAGCAA GTTGGGGAAC CAGTGGAATG GTGACAAGGC 540
CAGGTGGAGG CTGGCTGTAT TTTGGGGGCA TCCAGTGCCC CATCCTAAGA GCACCCTGAC 600
CTCCTTGGAG GAGATCGCCT TATGCCCGCT TCCCTCAAGG AGGGCCAAAG GGGTCATATC 660
CTTCCCAGCC AGCCCCAACC TGGGACAGGA ATGTGGCGTC CCCTGGCCAA TTGGTTGTTC 720
TTGCCTAGGG CTTTGGCTCC TGAGTGAGTG AGATGAGGAC ACTGGTGGTA AGAGGTCCTT 780
TATAAAAGCA GGTGCGGCAG CAGTGGCTGT GGCCCCGGGG TCCTGGCCGA GACTGGCTGA 840
CTGGCTTCCG TCCCCAGAGC CCTCACTTCC TGATTTTCCC AAGCCTGGTT TCCCCCTGTC 900
TATTGTCCAT TCTGTGAGCT CTCCCCACTG TGGACTTCCA TTAAATTCCC CGCTGCTTAA 960
ACTAGCCAGA GTCAGTTTCC TGCTCCCAGA CACAAGCATG GGCCTGAGTC AGCCGCTCAA 1020
CTGACGTCCG TGGAGTCAGC TGGAGTCTCT GCAGTTTGCT CCTCACAGTG CATCTTGAAC 1080
CTGATTCATT CCCCTGACCT CTCTCCAGAT CTGCATTTTC TCACTCCTGG GCAGCTGCAG 1140
CTGCTTCCAG CCTGGGCTTC CTCCCAGCTC TCTACATCCT AAGTTCTCTT AAGTATCACT 1200
GCTGGACTTT GGTCCTGCAG ACACCCCTGC TCAAGAAGTT CATGTGGCTC CCGCCGCCCA 1260
GTGGTCAAGT CCAGCGTCCA TAGCCTTCTG TAGCCCGGCC CTGCCCCCTG CCCCGTGACT 1320
GGAGAAGCCC TGTGTTCTTG AGGGGCTCCA GGCGGGTCAC CTTGCAGCCT TCTCCCAATG 1380
GAAAGCCTGT CCTAACCTTA GTGAGAGTTC AGGGTTGGGG GTTGGCTCTC TGGATCTGCG 1440
TCAGTGCTCC AAGCAACTGC CTTAGTGGGG CAGTCACTGA CCCCCCTGGA GTTGCTGCCA 1500
TCTACAGAAG GCCTGGGCTG GGTCAGGTGG CCGCTGGCCG TTCCTCACAG CGGAACGGAT 1560
GCTCTGCAAA GGCCCTCCTG ACTTTTGTTC ACTTCGTCCC TTTGTGAGGC CCCAGCCCTG 1620
GCAGAGGTCA TGGAGGGACC ATCCAAAGGC CCCGCCTTCT CCACCTTCAT CATTGCAATC 1680
CCATGAGCCA GGTGGGCACA GGTGGCTTGC ACTGTGGAAC CTCAGGAAAA AGGAGACAGG 1740
CATTGATGCC AGCCCCACAG AGGCACAGAG CTCTTCCTTG GCGCCTGCTG TGTGGACAAA 1800
GGCCTGGCCA GTGTGCGGAG TCTGGGGTTC TGTGATGCCA CAGGCCCTGC CTCTGTGTGA 1860
GCTGCTGCCT GCAGGGCCTC CCTCACCCTG CAGCCTCATC ACCTCCTGAC CATTGCAGGC 1920
AACCGACCAA GCTCTCGTGT GAGGTGGGCA CCCCCTGGGC TGTCTCTCCA GCTTACAAGA 1980
ATGGCCCCCT TTCAAGTCAT TGCCTTGAGC TGTCTAGACC CATCCAGGCA GGGTTTTAGC 2040
ACAAGGCTCT CAGGAGTTAA ACATGCCATG AAACATGCCC CACTTCCCAG GATATAATTA 2100
GACCAGAGTC CTCTCCCTGG GAGTGTGTGC GTGTCAGAGA GAGACAAAGA GAAAGAGAGG 2160
GAGGGAGGAA GGGAGGGAGG GAGGCGGAGA TTGGCTGAGG GCCTGTCTCT GGTTCGGGGC 2220
CTGTCACCCA TGAGCAGCTT GGCTCCCCGC TGAGTTCCCT CGCCTCTTGC CATTGGCAAG 2280
ACACACGGAG GAAGGCTCCT GCAGAGAAGA CAGACAGGCA AAGCTCCTCA GAGGGGAGCT 2340
GGCCAGGAGG CCCAGGCCTC ACCCACCCCG TCACTGTCCT GGCTCTGAGG CCATCCTCAC 2400
CCCTTGCTGC AGGGGCTTAC CCATCTCCAC TGGGTTAGGC TGTGTGCCCG ACTGGCCTTT 2460
TTCCTCTGGG TATTTGGGGC ATGCTCACCT GTGGACTAAT GTTTTTGAGA ACAAATTTTA 2520
AATGTTAATA GCCTTATTTT TTTTTTCTGA TAAAGTAATA GAGGAAAACA TTAAAAAGAG 2580
AGTAAATCTC CCTGCTTTGT TTTGCTTTGA GGGTCTGGCT CTGTTGCCCA GGCTGGAGTG 2640
CAGTGGCGCG ATCTCAGCTC ACTGCAGCCT TGACCTCCTG GGCTCAAGGG ATGCTCTCAC 2700
CTCAGCCTCT GGGACTAAAG GCATGTGCCA CGACACTCAG CTAATTTTGT TTAGTTTTCG 2760
TAGAGACGAG GTCTCACTAT GTTATCCAGG CTGGTCTCAA ACTCCTGGGC TCAAGCAATC 2820
CTCCCACCTT GGCCTCCCAA AGTTCTGAGA TTACAGGCAG GAGCCAAGGT GACTGGCCTA 2880
TTGTTAGTTT TTTAAAGTGT GATTGTAGTA 2910