EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-25782 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr14:100044640-100048120 
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
CATCAGTGTG TGTGTGTGTG TGTGTGTGTG TGTACACATC TCCACACCCA TACAGCCCGT 60
CCTGTATCCC CCATCGGTGT GTTTGTGTGT GTGTGTGAGT GTACACCTCT CCACACCCAT 120
ACAGCCCACA CCTATGTTCC CCGTCATGCA GTAGTTCTTA AATGGTAGTG ATGTGGTTGC 180
TTATTCAGTG TGTGTATGTC AACTCCCATC ACTGTGTGTG TGTGACTGTG CACATGTCTC 240
CACACCCACA TGGCCTGTAC CTATGTCCCC TGTCACTGTG TGTGTGAGCC TCCACAGCCT 300
GCACCCTCCT CTTGGTCATG TTCAATGATT TAAAAGCATC CCTCCCCACT GCTTCTATTT 360
TTGCTTTTGA CCTTTAGTTG AATGCTCACA GCTGCTGGGC CGTTGGCGTG ATGGTGAGTT 420
CATCACGTGT AATCGGGAGA CAGGACAATT TTATTTCCTC TAATACAAGC GCTGCTGCCC 480
CAGCCCCCTT CCAAGACCGG AGCTGGCTTC TCTAAGCGCT TCCCTAGAGT GAGGATGTAA 540
TAATCTGCTG GAAGGCGTGA CCGTGCCGTG GAAGGCTCTA GGTGACAGGT GGATGTGGTC 600
CGTGTCACCC TGCTGGTGTT GACACACTCC CTGCCCCACC TCCATCCACA AGCCCTGCTG 660
GGGCATGGAG GAGGGTGCTC TCTTACCAAC ACTTCGGGCT GAGAACCCAC AGACTCTCTC 720
CATTGCTCAT GAAGCCCCTA CTGCAGGTGA GGAAACTGAG GCACAGAGCC CAAGAGAGGT 780
GCTCAGGTCA CACCATGGAG GCCTGTCTGA CCCAGGTGGC CCTGAGTCCA GAGGTGCTCG 840
CCTGGGTACC CACACAGTCC CCTGGGCTCC TGAGTGCCTT TTCCCCCATG AAATGACGTC 900
AGGGAAACCC CCTGTCCTGG GGCTGAAGTT CTGCCTCCAG CCTTGGTGCC AAACAAGCCA 960
GAGAAGTGGC GGGGCTGCCC CAACAGGCAC CGTCCTGGAC GCAGTGTCCC TGTGCACACC 1020
TGTGGAACCT GCTCTGCCGG TGGAGGAAGA GAAGTGGGGG AGGGGGGCAG GGAGGCCCAG 1080
TGTGACTCCG AGTCTGCTGT GGGCTCAGAG ATACTCACAC AGTGAGTGGG ACCTACAGGG 1140
GAGCTGGCAG GGGCCTGGGG TTGGGGGCTC CCCCTATCCT GCCCTCCCAG CCCTGGTCCT 1200
TCTGCCCAGA TCCCAGGGCA TGTGTTCCCA GCTGCCCCAC TGACTGCCTC ACTCCCAACT 1260
CTTCCTGGAG CCTTCTCCAG GGCGCAGCCC CAGACAGCCC AGGCAAGAAA CCCAGAAGGA 1320
AGAGGTGGGG CCAGAAAGGT GAGGACTGGA TTCGGGATTG AGGTGGGGGC TATGGTCAGC 1380
TCCCTGGGGG AGGCAGCGGG AGGCAGGGGC AGGCCTGGGG GAGTCCAGGG CAGCGGGGGA 1440
GAGGTCCCCA CATGTCAGCT CCTGCCTGCT GTCACCTCTC CTGATTCCTT CCCCATCCCA 1500
CTCAGGAGTG GGGATGGGGG ATCCCATCTC ACTAATGAGG AAACTGAGAC ACACACGGTT 1560
GTTGGTCGTT AGGCTGTCTA CCAGAGGTCG CCCAAGGCCA GGCCACCCTG CCCACCCCCG 1620
TCTGGCTCAG TCCAAGACTT TGGGAGTCTT GGCCAGGGTA GGGCATTAAT CACCTCAGCA 1680
GCGGACCACC ATGACAAACC CCACATACCC CACATACCCC GGAGTGAGTC ACATGGGCAG 1740
GGCTGGCCCC TTCCTCTTGG TCTCACATTC CTAAACAGTA GACACCTTCC AGGAATTCGG 1800
TCAGCAAAGT GGCTGGAGCT GCTGGGACAG ACAGCCTGTG CAGGCCTGGC CCCCGGCACA 1860
CCCAGAGGAA GGAGAGGCTG GGTGGCTCAG GTGTGGCCCC GGAGCTCGGC AGGCCCAGCC 1920
CCCAGGGACA CAGCCCACGT GCACAGTGGG TGACAGACCA GCTAAGATAT AGTGCTGTCC 1980
TAAGAGCTCA AGGCAGAGAC TGCCATTAAC ACAGCCCAGC CCAGACAGAA GAGCACACCT 2040
CCCAGAGTCA CCGTGAGTGC AGTGGGGGAG GCAGGAGGGG CTTTTGGACA CTGAGGTAGC 2100
TGGAAAAGCA AGCAGAGGGC GGCATCTCAG CCACAGGCTG GAGACATGAG GGACGTCCCC 2160
AGTGAGGGGA GGGGGGGAAG GGGGCGGGGA TGGGGGGAAC TGGAGGCGGA GAAGACAGCC 2220
AGGGAAAGAG GGGAGGTATG AAAACGCCTG GCTAATGGTG TTAAGGAACT GCCACTCATG 2280
GCCGGGCATG GTGGCTCACG TCTGTAATCC CAGCACTTTG GGAGGCCAAG GTGTGTGGCT 2340
CATTTGACGT CAGGAGTTCA AGACCAGCCT GGCCAACATG GTGAAACCCC ACCTCTGCTA 2400
AAATTACAAA AATTAGCTGG GCATGGTGGC GGGCACCTAT AGTCCCAGTT ACTTGGGAGG 2460
CTGAAGCAGG AGAATGGCTT GAACCCGGGA GGCAGAGGTT GCAGTGAGCC AAGATCGCGC 2520
GACTGCACTC TAGCCTGGGT GATAGAGCAA GACTCCATCT CAAGAAAATT AAAAAGGAAC 2580
TGCTGTTCAT CTTCTTCCAG AAGACATGGG AGAGGAATGT GGCAAAGGCA TCAGAGCCTG 2640
ATCACAGAGC ACCTCCAACT TTATTTTCAG AATCCTGAAC CTGATGCTGA GGGGTCCCCA 2700
GAGAGCCAAG TGCAGGGTAG GGGCTGTGTT TCAGGAAAGA CAGAGTGAGG GCTGGAGGAG 2760
ACCATCCTGG AGGCAGGGAG GCCAGCTGGG AGGCTGGTTC CACGATCGCT GAAGCAAAGA 2820
GGAGGAGTGG GAGGGTGAAA CCCCACCATC AGCACTGGAG AAGGAATGGC AGGTGTGCCC 2880
AGTGCCACCC TACCCTGGCA AAGGCCACAC CCATGCTCAA ACCACTGGGC TCTCCAGGGC 2940
AAAGACCTGG GCAAGGCAGG ATGGACAGGG CCTGGTCAAC CCAGAGCCCC GTGAACAGAC 3000
CACCAACTAT GCCACACCAA GCTGGTCAGA CCCACCAGAT GCTGGACCCC GCCTGCAAAG 3060
AACACAGCCC CTGAAGACAA CCGTGGAAGT TCTATCTTCC AGGACAGAGC TGCCAGGTAG 3120
GAGGACAGCG TATGAAGCCT CACACCTGGG GTCTGGCCTC GCTCCCCCCA CCCATGGTCA 3180
CTCACGGCCA CTCCACGGGT GGGCAGAAAC CCAGTGACCG GTGCAGGCCT GCCTGCCTGG 3240
CCTGGGGCGT CCATGACCCC TGCCTCGGCC ACCGCACAAT CGCTCCCTTT GTTCCCCGGC 3300
TCCCCATTGT CTGCAATTCT CTCGCCTGCC TGCGCCAGGC CAAAGGAGGA TTTCCAGGGG 3360
GATTTCTCAA TGGGCTCGCA GGGAAACAAC CTGGCAGTGG GACCTGCTGC TCATGGCCTT 3420
CCTTGAAAGG CCACGAAGCA GGATGGGGGC TGACGACCCT TTGTAAATGG CCCCAGATGT 3480