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

TagContent
EnhancerAtlas ID
HS047-10756 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr14:100044680-100048130 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr14:100047542-100047553GGCCACACCCA+6.62
SP2MA0516.2chr14:100046817-100046834AAGGGGGCGGGGATGGG-6.04
ZNF263MA0528.1chr14:100045681-100045702GGAGGAAGAGAAGTGGGGGAG+6.04
ZNF263MA0528.1chr14:100045695-100045716GGGGGAGGGGGGCAGGGAGGC+6.11
ZNF263MA0528.1chr14:100045678-100045699GGTGGAGGAAGAGAAGTGGGG+6.69
ZNF263MA0528.1chr14:100046804-100046825AGGGGAGGGGGGGAAGGGGGC+6.75
ZNF263MA0528.1chr14:100047457-100047478AGAGGAGGAGTGGGAGGGTGA+7.04
ZfxMA0146.2chr14:100046480-100046494CAGGCCTGGCCCCC-6.25
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00922chr14:100044482-100046601Adrenal_Gland
SE_06477chr14:100047173-100049145Brain_Hippocampus_Middle
SE_23140chr14:100040149-100047008Colon_Crypt_1
SE_23140chr14:100047165-100047974Colon_Crypt_1
SE_23807chr14:100044472-100047038Colon_Crypt_2
SE_23807chr14:100047221-100047760Colon_Crypt_2
SE_24879chr14:100044342-100047065Colon_Crypt_3
SE_24879chr14:100047217-100048129Colon_Crypt_3
SE_26586chr14:100036268-100048060Esophagus
SE_27780chr14:100044621-100047720Fetal_Intestine
SE_28740chr14:100044751-100047885Fetal_Intestine_Large
SE_31455chr14:100044168-100048125Gastric
SE_40985chr14:100034161-100047061Left_Ventricle
SE_41558chr14:100034157-100047015LNCaP
SE_41558chr14:100047183-100048847LNCaP
SE_42529chr14:100036484-100047048Lung
SE_47508chr14:100044802-100046802Pancreas
SE_47508chr14:100047193-100047929Pancreas
SE_49276chr14:100037919-100046958Right_Atrium
SE_50321chr14:100044222-100047023Sigmoid_Colon
SE_52517chr14:100044484-100047012Small_Intestine
SE_54552chr14:100023051-100046861Stomach_Smooth_Muscle
SE_54552chr14:100047097-100048205Stomach_Smooth_Muscle
SE_57311chr14:100043817-100047007VACO_400
SE_61471chr14:100013991-100069569Toledo
SE_65289chr14:100044656-100048217Pancreatic_islets
SE_68735chr14:100045019-100046812H9
SE_68735chr14:100047264-100048227H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14100045606100045757
Number: 1             
IDChromosomeStartEnd
GH14I099578chr14100044558100048013
Enhancer Sequence
TCCACACCCA TACAGCCCGT CCTGTATCCC CCATCGGTGT GTTTGTGTGT GTGTGTGAGT 60
GTACACCTCT CCACACCCAT ACAGCCCACA CCTATGTTCC CCGTCATGCA GTAGTTCTTA 120
AATGGTAGTG ATGTGGTTGC TTATTCAGTG TGTGTATGTC AACTCCCATC ACTGTGTGTG 180
TGTGACTGTG CACATGTCTC CACACCCACA TGGCCTGTAC CTATGTCCCC TGTCACTGTG 240
TGTGTGAGCC TCCACAGCCT GCACCCTCCT CTTGGTCATG TTCAATGATT TAAAAGCATC 300
CCTCCCCACT GCTTCTATTT TTGCTTTTGA CCTTTAGTTG AATGCTCACA GCTGCTGGGC 360
CGTTGGCGTG ATGGTGAGTT CATCACGTGT AATCGGGAGA CAGGACAATT TTATTTCCTC 420
TAATACAAGC GCTGCTGCCC CAGCCCCCTT CCAAGACCGG AGCTGGCTTC TCTAAGCGCT 480
TCCCTAGAGT GAGGATGTAA TAATCTGCTG GAAGGCGTGA CCGTGCCGTG GAAGGCTCTA 540
GGTGACAGGT GGATGTGGTC CGTGTCACCC TGCTGGTGTT GACACACTCC CTGCCCCACC 600
TCCATCCACA AGCCCTGCTG GGGCATGGAG GAGGGTGCTC TCTTACCAAC ACTTCGGGCT 660
GAGAACCCAC AGACTCTCTC CATTGCTCAT GAAGCCCCTA CTGCAGGTGA GGAAACTGAG 720
GCACAGAGCC CAAGAGAGGT GCTCAGGTCA CACCATGGAG GCCTGTCTGA CCCAGGTGGC 780
CCTGAGTCCA GAGGTGCTCG CCTGGGTACC CACACAGTCC CCTGGGCTCC TGAGTGCCTT 840
TTCCCCCATG AAATGACGTC AGGGAAACCC CCTGTCCTGG GGCTGAAGTT CTGCCTCCAG 900
CCTTGGTGCC AAACAAGCCA GAGAAGTGGC GGGGCTGCCC CAACAGGCAC CGTCCTGGAC 960
GCAGTGTCCC TGTGCACACC TGTGGAACCT GCTCTGCCGG TGGAGGAAGA GAAGTGGGGG 1020
AGGGGGGCAG GGAGGCCCAG TGTGACTCCG AGTCTGCTGT GGGCTCAGAG ATACTCACAC 1080
AGTGAGTGGG ACCTACAGGG GAGCTGGCAG GGGCCTGGGG TTGGGGGCTC CCCCTATCCT 1140
GCCCTCCCAG CCCTGGTCCT TCTGCCCAGA TCCCAGGGCA TGTGTTCCCA GCTGCCCCAC 1200
TGACTGCCTC ACTCCCAACT CTTCCTGGAG CCTTCTCCAG GGCGCAGCCC CAGACAGCCC 1260
AGGCAAGAAA CCCAGAAGGA AGAGGTGGGG CCAGAAAGGT GAGGACTGGA TTCGGGATTG 1320
AGGTGGGGGC TATGGTCAGC TCCCTGGGGG AGGCAGCGGG AGGCAGGGGC AGGCCTGGGG 1380
GAGTCCAGGG CAGCGGGGGA GAGGTCCCCA CATGTCAGCT CCTGCCTGCT GTCACCTCTC 1440
CTGATTCCTT CCCCATCCCA CTCAGGAGTG GGGATGGGGG ATCCCATCTC ACTAATGAGG 1500
AAACTGAGAC ACACACGGTT GTTGGTCGTT AGGCTGTCTA CCAGAGGTCG CCCAAGGCCA 1560
GGCCACCCTG CCCACCCCCG TCTGGCTCAG TCCAAGACTT TGGGAGTCTT GGCCAGGGTA 1620
GGGCATTAAT CACCTCAGCA GCGGACCACC ATGACAAACC CCACATACCC CACATACCCC 1680
GGAGTGAGTC ACATGGGCAG GGCTGGCCCC TTCCTCTTGG TCTCACATTC CTAAACAGTA 1740
GACACCTTCC AGGAATTCGG TCAGCAAAGT GGCTGGAGCT GCTGGGACAG ACAGCCTGTG 1800
CAGGCCTGGC CCCCGGCACA CCCAGAGGAA GGAGAGGCTG GGTGGCTCAG GTGTGGCCCC 1860
GGAGCTCGGC AGGCCCAGCC CCCAGGGACA CAGCCCACGT GCACAGTGGG TGACAGACCA 1920
GCTAAGATAT AGTGCTGTCC TAAGAGCTCA AGGCAGAGAC TGCCATTAAC ACAGCCCAGC 1980
CCAGACAGAA GAGCACACCT CCCAGAGTCA CCGTGAGTGC AGTGGGGGAG GCAGGAGGGG 2040
CTTTTGGACA CTGAGGTAGC TGGAAAAGCA AGCAGAGGGC GGCATCTCAG CCACAGGCTG 2100
GAGACATGAG GGACGTCCCC AGTGAGGGGA GGGGGGGAAG GGGGCGGGGA TGGGGGGAAC 2160
TGGAGGCGGA GAAGACAGCC AGGGAAAGAG GGGAGGTATG AAAACGCCTG GCTAATGGTG 2220
TTAAGGAACT GCCACTCATG GCCGGGCATG GTGGCTCACG TCTGTAATCC CAGCACTTTG 2280
GGAGGCCAAG GTGTGTGGCT CATTTGACGT CAGGAGTTCA AGACCAGCCT GGCCAACATG 2340
GTGAAACCCC ACCTCTGCTA AAATTACAAA AATTAGCTGG GCATGGTGGC GGGCACCTAT 2400
AGTCCCAGTT ACTTGGGAGG CTGAAGCAGG AGAATGGCTT GAACCCGGGA GGCAGAGGTT 2460
GCAGTGAGCC AAGATCGCGC GACTGCACTC TAGCCTGGGT GATAGAGCAA GACTCCATCT 2520
CAAGAAAATT AAAAAGGAAC TGCTGTTCAT CTTCTTCCAG AAGACATGGG AGAGGAATGT 2580
GGCAAAGGCA TCAGAGCCTG ATCACAGAGC ACCTCCAACT TTATTTTCAG AATCCTGAAC 2640
CTGATGCTGA GGGGTCCCCA GAGAGCCAAG TGCAGGGTAG GGGCTGTGTT TCAGGAAAGA 2700
CAGAGTGAGG GCTGGAGGAG ACCATCCTGG AGGCAGGGAG GCCAGCTGGG AGGCTGGTTC 2760
CACGATCGCT GAAGCAAAGA GGAGGAGTGG GAGGGTGAAA CCCCACCATC AGCACTGGAG 2820
AAGGAATGGC AGGTGTGCCC AGTGCCACCC TACCCTGGCA AAGGCCACAC CCATGCTCAA 2880
ACCACTGGGC TCTCCAGGGC AAAGACCTGG GCAAGGCAGG ATGGACAGGG CCTGGTCAAC 2940
CCAGAGCCCC GTGAACAGAC CACCAACTAT GCCACACCAA GCTGGTCAGA CCCACCAGAT 3000
GCTGGACCCC GCCTGCAAAG AACACAGCCC CTGAAGACAA CCGTGGAAGT TCTATCTTCC 3060
AGGACAGAGC TGCCAGGTAG GAGGACAGCG TATGAAGCCT CACACCTGGG GTCTGGCCTC 3120
GCTCCCCCCA CCCATGGTCA CTCACGGCCA CTCCACGGGT GGGCAGAAAC CCAGTGACCG 3180
GTGCAGGCCT GCCTGCCTGG CCTGGGGCGT CCATGACCCC TGCCTCGGCC ACCGCACAAT 3240
CGCTCCCTTT GTTCCCCGGC TCCCCATTGT CTGCAATTCT CTCGCCTGCC TGCGCCAGGC 3300
CAAAGGAGGA TTTCCAGGGG GATTTCTCAA TGGGCTCGCA GGGAAACAAC CTGGCAGTGG 3360
GACCTGCTGC TCATGGCCTT CCTTGAAAGG CCACGAAGCA GGATGGGGGC TGACGACCCT 3420
TTGTAAATGG CCCCAGATGT GAGCAGCTAT 3450