EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS176-17256 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr17:71286700-71289110 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr17:71288636-71288656TGTGGGGGGTGGGGGTGGGG-6.17
RUNX1MA0002.2chr17:71287012-71287023AAACCACAGAC-6.62
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00203chr17:71281786-71292211Adipose_Nuclei
SE_00919chr17:71280759-71290474Adrenal_Gland
SE_01949chr17:71286022-71290366Aorta
SE_02957chr17:71286918-71287765Bladder
SE_02957chr17:71287829-71289133Bladder
SE_04533chr17:71284556-71288674Brain_Anterior_Caudate
SE_06356chr17:71277769-71290798Brain_Hippocampus_Middle
SE_23373chr17:71285973-71289030Colon_Crypt_1
SE_23953chr17:71286005-71288922Colon_Crypt_2
SE_24951chr17:71286071-71288667Colon_Crypt_3
SE_26142chr17:71284616-71290403Duodenum_Smooth_Muscle
SE_26892chr17:71286041-71290403Esophagus
SE_28228chr17:71284304-71287350Fetal_Intestine
SE_28228chr17:71287427-71288323Fetal_Intestine
SE_31497chr17:71284450-71290426Gastric
SE_34366chr17:71286076-71290834HCT-116
SE_34727chr17:71283787-71290955HeLa
SE_40779chr17:71281080-71291827Left_Ventricle
SE_41738chr17:71286058-71288619LNCaP
SE_42276chr17:71282392-71290554Lung
SE_44396chr17:71285868-71289101NHDF-Ad
SE_45062chr17:71286886-71289026NHLF
SE_46731chr17:71286078-71286970Ovary
SE_46731chr17:71286991-71288670Ovary
SE_47498chr17:71286740-71289028Pancreas
SE_48667chr17:71282058-71290313Right_Atrium
SE_49576chr17:71286813-71289033Right_Ventricle
SE_50297chr17:71283561-71288835Sigmoid_Colon
SE_52570chr17:71282759-71290321Small_Intestine
SE_53786chr17:71283801-71289650Spleen
SE_54836chr17:71279223-71290708Stomach_Smooth_Muscle
SE_57720chr17:71287754-71288504VACO_503
SE_65340chr17:71280793-71290305Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177128715571288873
Number: 1             
IDChromosomeStartEnd
GH17I073287chr177128403471291744
Enhancer Sequence
AACAAGCAAA ACTGTCTCAA GATATTGCCC AATGTCCCCC AGGAGGCAAA ACTGCCCCAG 60
TTGAGAAACA GCAGCCTTGA GTGAGAACAC ACAGGTGAAG ATAGAGCAGG TATGCTCACC 120
AGGTAAACAA CAAAGACAGA GAAGCAGGGA GGCGGGTGTG GATGGTCAGA ACCGGGTGAG 180
AACATGGCGG CACGAGCCCC CAGAGCTGCG TTAAGGGTTT CAACGCCAAG GCAGGAACCC 240
CCAGACCCTG TGAGTGATGT CAGGTCCTGT GGTTTCCCGA TCTTATACGC TCATTAGAGA 300
GGAAAGAAAG GGAAACCACA GACCCGGCTC CCCAGGACTC ACCAGAGAAG CTGCAGGTCA 360
CTGTGGCTGC CCAAAGGGAC CAAATATCCT GGCCATGATG GCTACAGGGG AGGACAGCTC 420
CCCGCATCCC ATTAGCCACA CCACCCAGCA CATCCTTGCG GGTAGAACTA TTGAGGTAGG 480
TCAGAGGGGA CAGCAGGGAA ACTCAGCTGA AATCACGGCC ATCCTGGGCT AGCCCTGGGG 540
TCCCCAGGAT CTTGTTCAAC CCCACACCCC AGAAAGACAG GGACAGGTCT ACCCAGTGCT 600
GCCTGCTGCC ACGGTCTCGC TTCCTGGGGG GTTGGGAACG AGACTTTGTG GCTTGTAGAA 660
AGCCATCTTC AATAACCAGC AAGGAAGGGT CCTGAGAGAG TTGGGGCCTA GAGGGAGTCA 720
CGCATCTGTC CCACTGCCCC AGCGAGGAGG GGGCTGCAGT ACCTGGCAGT CCACACTGGG 780
GATGAGGCCT GGGTGTCTGG AGCTCAGACT AGACAGGCCA CCCAGCAGGA TTGAGGGTCA 840
GCAACAGCTT GGTTTCACCA GCCTTGAGTG ACCTTGAGTC ACTCTGAGCT TCTAACAGAG 900
AACAGTTTGG AGGTGACGAG CTGGATCATA GAGTTTAAGA GAAAGTAGGT GGTGGGAGTC 960
TCGCCAGAGG CCTGGGCAGG TCCTGGGGGC AGCTATGGTT TGGGAGGCCA CAGGGCATTG 1020
TGGCTTTGGG CGGGGCTTTC AGAAGCATGG TGACTCAGCT CTGGGGAAGT GGCTAAAATA 1080
GGCTGCCCAA CGTGGGGCAG GCACTCCCCA TAGCCTGCCT TGGGCGGGAC ACCCCCACCC 1140
CACCCCAGAA ACCACATCCC ACTTTCTTGG CAGGGAGAGG GAAAATGGAT CACAGCTCAC 1200
AGCCCTCCCT AGCTCTCCTG AGCCTCCGGA GGAACAGATT CCTCTACCCT CAGCCCACTG 1260
ACCACGGAAC CTTCCTTTAA GGTGGGAACG AGGAGCCCTC CCCAGAAGGT CAGGCCCCTG 1320
CTTGGGTCAC AGCAACCACA CCTTTAGTTC AGCCCTGTTC CTGAGACTAC GGAAGACCAC 1380
CCTTGCCTGG ACCCCTCGCC TATCCTCCCT GGCCCTCCCA GCTTGGCCAG CCCAGCAGAC 1440
CCAGAGCAGA AGGACAGACG GGACCAACAC TTCTCACTCC AAGTGACCGG GCAGTGGCCT 1500
GTCCCTGGCA GCTTGGCTTG AGGCAGGCGC CAGACCTGAG CTCTCATGGG GCAGCTAGGC 1560
AGGCCTCGCT CTCTGAAGCT GCCCTGCGGT TCACCCCGGT ATACAGGGTA CACAACATGC 1620
CTCAATGCCC ACTGCCACTG CCTCCGCCAC TGCTGCTGGG CAGCATGCCC TCTGCAGGGC 1680
CTTCCCCTAG CTGTTCTAAC CAACCACCCG ATGCCAGGTC CAGGCAATGT GGCCGAATAG 1740
CAGAGGGCTT TTAGTGCACG ATGACTTTAG TTGTGACCTG GATCGGCTAC AAGAGGCTTT 1800
GTTCCATTAC TCATCATCCA GTCACTCACT CCATGACTTC CTGCAGACCC ACTGATATTC 1860
ACAAACTCTT CTAGGCCCTG GAGATAGAGC AGTGAAAATA GCACGCTGTT TTCCCAGGGC 1920
ACGTGTGTAG TGTGAGTGTG GGGGGTGGGG GTGGGGAATG GAGGTGTAAA CCTATAAATA 1980
AAATAAATGG TATCTCATAT TCCTCAGTAT AAGGAGGGAA AGGGGTGGTA TGAGTGGGTG 2040
TGGGAGTCAG GGGGTCTGGG GGAGGCCCCT CTTGAGGAAG GAGCATCATG AGTTGAGAAC 2100
CAAATGATGA GAAGGAACCA GCCGGGTCAG AAGCGACCCA GGCAGAGGGA ACGGCGCGTG 2160
CAAACGCCGG GGTATAGGAA CAGGCTTGTG GCATTTATGG AATAGAATAA AAATCCATGC 2220
AGCCAGGGCC CAGGTTACAT AGAGCCCTCC CTACCAGGCC ACATAAAGAG TTCTGTTTTG 2280
TTTTTAGTTT TTATTACAGG CACCTGCCAT CATGCCCAGT TAATTTTTGA ATTTTTTGGA 2340
GAGACCAGGT TTCACCATGT TGGCTAGGCT GGTCCTGAAC TCCTGACTTC AGGTGATCTG 2400
CCCGCCTCGG 2410