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

TagContent
EnhancerAtlas ID
HS054-02810 
Organism
Homo sapiens 
Tissue/cell
FT246 
Coordinate
chr17:71286840-71290270 
Target genes
Number: 3             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr17:71288636-71288656TGTGGGGGGTGGGGGTGGGG-6.17
RUNX1MA0002.2chr17:71287012-71287023AAACCACAGAC-6.62
ZfxMA0146.2chr17:71289100-71289114CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 40             
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_04533chr17:71289128-71290063Brain_Anterior_Caudate
SE_06356chr17:71277769-71290798Brain_Hippocampus_Middle
SE_23373chr17:71285973-71289030Colon_Crypt_1
SE_23953chr17:71286005-71288922Colon_Crypt_2
SE_23953chr17:71289282-71290185Colon_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_41738chr17:71289449-71290021LNCaP
SE_42276chr17:71282392-71290554Lung
SE_44396chr17:71285868-71289101NHDF-Ad
SE_45062chr17:71286886-71289026NHLF
SE_45062chr17:71289070-71290349NHLF
SE_46731chr17:71286991-71288670Ovary
SE_46731chr17:71289254-71289824Ovary
SE_47498chr17:71286740-71289028Pancreas
SE_47498chr17:71289077-71290268Pancreas
SE_48667chr17:71282058-71290313Right_Atrium
SE_49576chr17:71286813-71289033Right_Ventricle
SE_49576chr17:71289092-71289797Right_Ventricle
SE_50297chr17:71283561-71288835Sigmoid_Colon
SE_50297chr17:71289197-71290314Sigmoid_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: 2             
ChromosomeStartEnd
chr177128715571288873
chr177128918171290204
Number: 1             
IDChromosomeStartEnd
GH17I073287chr177128403471291744
Enhancer Sequence
GAAGCAGGGA GGCGGGTGTG GATGGTCAGA ACCGGGTGAG AACATGGCGG CACGAGCCCC 60
CAGAGCTGCG TTAAGGGTTT CAACGCCAAG GCAGGAACCC CCAGACCCTG TGAGTGATGT 120
CAGGTCCTGT GGTTTCCCGA TCTTATACGC TCATTAGAGA GGAAAGAAAG GGAAACCACA 180
GACCCGGCTC CCCAGGACTC ACCAGAGAAG CTGCAGGTCA CTGTGGCTGC CCAAAGGGAC 240
CAAATATCCT GGCCATGATG GCTACAGGGG AGGACAGCTC CCCGCATCCC ATTAGCCACA 300
CCACCCAGCA CATCCTTGCG GGTAGAACTA TTGAGGTAGG TCAGAGGGGA CAGCAGGGAA 360
ACTCAGCTGA AATCACGGCC ATCCTGGGCT AGCCCTGGGG TCCCCAGGAT CTTGTTCAAC 420
CCCACACCCC AGAAAGACAG GGACAGGTCT ACCCAGTGCT GCCTGCTGCC ACGGTCTCGC 480
TTCCTGGGGG GTTGGGAACG AGACTTTGTG GCTTGTAGAA AGCCATCTTC AATAACCAGC 540
AAGGAAGGGT CCTGAGAGAG TTGGGGCCTA GAGGGAGTCA CGCATCTGTC CCACTGCCCC 600
AGCGAGGAGG GGGCTGCAGT ACCTGGCAGT CCACACTGGG GATGAGGCCT GGGTGTCTGG 660
AGCTCAGACT AGACAGGCCA CCCAGCAGGA TTGAGGGTCA GCAACAGCTT GGTTTCACCA 720
GCCTTGAGTG ACCTTGAGTC ACTCTGAGCT TCTAACAGAG AACAGTTTGG AGGTGACGAG 780
CTGGATCATA GAGTTTAAGA GAAAGTAGGT GGTGGGAGTC TCGCCAGAGG CCTGGGCAGG 840
TCCTGGGGGC AGCTATGGTT TGGGAGGCCA CAGGGCATTG TGGCTTTGGG CGGGGCTTTC 900
AGAAGCATGG TGACTCAGCT CTGGGGAAGT GGCTAAAATA GGCTGCCCAA CGTGGGGCAG 960
GCACTCCCCA TAGCCTGCCT TGGGCGGGAC ACCCCCACCC CACCCCAGAA ACCACATCCC 1020
ACTTTCTTGG CAGGGAGAGG GAAAATGGAT CACAGCTCAC AGCCCTCCCT AGCTCTCCTG 1080
AGCCTCCGGA GGAACAGATT CCTCTACCCT CAGCCCACTG ACCACGGAAC CTTCCTTTAA 1140
GGTGGGAACG AGGAGCCCTC CCCAGAAGGT CAGGCCCCTG CTTGGGTCAC AGCAACCACA 1200
CCTTTAGTTC AGCCCTGTTC CTGAGACTAC GGAAGACCAC CCTTGCCTGG ACCCCTCGCC 1260
TATCCTCCCT GGCCCTCCCA GCTTGGCCAG CCCAGCAGAC CCAGAGCAGA AGGACAGACG 1320
GGACCAACAC TTCTCACTCC AAGTGACCGG GCAGTGGCCT GTCCCTGGCA GCTTGGCTTG 1380
AGGCAGGCGC CAGACCTGAG CTCTCATGGG GCAGCTAGGC AGGCCTCGCT CTCTGAAGCT 1440
GCCCTGCGGT TCACCCCGGT ATACAGGGTA CACAACATGC CTCAATGCCC ACTGCCACTG 1500
CCTCCGCCAC TGCTGCTGGG CAGCATGCCC TCTGCAGGGC CTTCCCCTAG CTGTTCTAAC 1560
CAACCACCCG ATGCCAGGTC CAGGCAATGT GGCCGAATAG CAGAGGGCTT TTAGTGCACG 1620
ATGACTTTAG TTGTGACCTG GATCGGCTAC AAGAGGCTTT GTTCCATTAC TCATCATCCA 1680
GTCACTCACT CCATGACTTC CTGCAGACCC ACTGATATTC ACAAACTCTT CTAGGCCCTG 1740
GAGATAGAGC AGTGAAAATA GCACGCTGTT TTCCCAGGGC ACGTGTGTAG TGTGAGTGTG 1800
GGGGGTGGGG GTGGGGAATG GAGGTGTAAA CCTATAAATA AAATAAATGG TATCTCATAT 1860
TCCTCAGTAT AAGGAGGGAA AGGGGTGGTA TGAGTGGGTG TGGGAGTCAG GGGGTCTGGG 1920
GGAGGCCCCT CTTGAGGAAG GAGCATCATG AGTTGAGAAC CAAATGATGA GAAGGAACCA 1980
GCCGGGTCAG AAGCGACCCA GGCAGAGGGA ACGGCGCGTG CAAACGCCGG GGTATAGGAA 2040
CAGGCTTGTG GCATTTATGG AATAGAATAA AAATCCATGC AGCCAGGGCC CAGGTTACAT 2100
AGAGCCCTCC CTACCAGGCC ACATAAAGAG TTCTGTTTTG TTTTTAGTTT TTATTACAGG 2160
CACCTGCCAT CATGCCCAGT TAATTTTTGA ATTTTTTGGA GAGACCAGGT TTCACCATGT 2220
TGGCTAGGCT GGTCCTGAAC TCCTGACTTC AGGTGATCTG CCCGCCTCGG CCTCCCAAAG 2280
TGCTGGGATT ACAGGAGCCA CTGCTCCTGG CCGATTTTTT TATGTTTTTA GAGATGGGGT 2340
TTCACCACGT CGGCCAGGCT GGTCTCGAAC TCCTGGCATC AAGCAATCCA CCCGCCTTGG 2400
CCTCCCAAAG TTCTGGCATT ACAGGCATGA GCCACCGCAC CCAGCCCAGG TAAGGAGTTT 2460
GGAGGTCATT ATAGGTGTAC AAGGAAACCG GCGGCTGTTT GTAAGCAGGC GAGTGATTCA 2520
ATCTGTGTAT CTGGAAGCTC CCGGAGGTCC TGGCATTGGA GGAATGAAGG AGGGGAGCTG 2580
GAATTCAGTC AGGAGGCTGT TGCAGAAATG CAGGTCAAAG AGGATGGAGA CCAGGATGTG 2640
GGTCTGGCGA AGGGGGACAC AGTGGGAGAC ATTTAGGCCA TGTTTTGGAG GTAGAGACAC 2700
CCGGGATTGT GGAGGGCCCA GACCAGGGAG GAGAGAAAAG ACAGGATCAA ATGGGACTCC 2760
AGGCCTTCCA GGGGCAGCCT CTGGTCCTGG CCATCCTTTC CCAGGTTTTG CCTGGCAGGC 2820
CACGGCCCCT TCTCACAGGA GGGGCTGACA TCCTACCCCT AGGCGGAACT TCACTTTGCC 2880
GAAACACAGG TGGCATTCTG CTACACAAGG CTTGTCAGAT GGAACAGCAC GCTGGAGGGG 2940
GTTGTGCAAG AGGCTCACTG GGACATGGGC CACAACTCTA AGAGGTGAGG GACTCTGGCT 3000
TTAGTCACCA GAGAAAAATC CAGTACTTTC TGGAACACTC ACCAGCCTTA CCCTGCAAAG 3060
ATAGGAAAGC ACAGGGAAGG CGGAAGACTG TGTTTCATTC AAACTGTGGC AGGGCTGAGG 3120
GCAGCTAAGT GAATGGGCGA GAACAGTGAC CGCTTAGATA CACGTGGTTA CATGTTCCAG 3180
GCAGGACTTC AATGCCGACT GTGTTGTGAT TTTAGCTGAC TTTAGTATTC TTGGGGATCT 3240
TTTAACTCCT TCATGTGCCC TGCTCAAAAG CCCTTGCATC TGGAAGTGTG CTGCGTGCGC 3300
AAGGAGGTTA AGGCTCACTG CTGTAATATT CTGAGCCTAA GTAACCACAA TCAAAAACCA 3360
AACACAAGGC CGGGCGTGGT GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCTGAGGC 3420
GGGTGGATCT 3430