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

TagContent
EnhancerAtlas ID
HS092-16507 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr14:74240790-74243560 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZfxMA0146.2chr14:74243535-74243549GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00050chr14:74240654-74243603Adipose_Nuclei
SE_01593chr14:74240742-74243055Aorta
SE_03933chr14:74240664-74242956Brain_Anterior_Caudate
SE_04955chr14:74240713-74242377Brain_Cingulate_Gyrus
SE_05881chr14:74240543-74243402Brain_Hippocampus_Middle
SE_09248chr14:74240726-74242465CD14
SE_10252chr14:74241278-74242407CD19_Primary
SE_10947chr14:74233901-74245970CD20
SE_13333chr14:74241800-74243369CD34_Primary_RO01536
SE_14441chr14:74240524-74241829CD4_Memory_Primary_7pool
SE_14441chr14:74241833-74243125CD4_Memory_Primary_7pool
SE_17393chr14:74240572-74243432CD4p_CD25-_CD45RAp_Naive
SE_17831chr14:74240828-74243379CD4p_CD25-_CD45ROp_Memory
SE_18433chr14:74240430-74243324CD4p_CD25-_Il17-_PMAstim_Th
SE_19223chr14:74240852-74242573CD4p_CD25-_Il17p_PMAstim_Th17
SE_20160chr14:74240695-74241883CD56
SE_22379chr14:74239927-74243400CD8_primiary
SE_23064chr14:74240912-74241746Colon_Crypt_1
SE_23727chr14:74240749-74241886Colon_Crypt_2
SE_24718chr14:74241276-74241844Colon_Crypt_3
SE_25792chr14:74241423-74243271Duodenum_Smooth_Muscle
SE_26529chr14:74240779-74243025Esophagus
SE_27618chr14:74240627-74241940Fetal_Intestine
SE_28542chr14:74240580-74242022Fetal_Intestine_Large
SE_31388chr14:74239905-74243015Gastric
SE_40688chr14:74240662-74243132Left_Ventricle
SE_42108chr14:74240624-74243479Lung
SE_44659chr14:74241744-74243169NHDF-Ad
SE_48076chr14:74240531-74243025Psoas_Muscle
SE_50054chr14:74240723-74243627Sigmoid_Colon
SE_51191chr14:74240960-74243306Skeletal_Muscle
SE_52341chr14:74240670-74243518Small_Intestine
SE_53290chr14:74240691-74243216Spleen
SE_58664chr14:74207642-74255391Ly1
SE_59257chr14:74219698-74251676Ly3
SE_59926chr14:74207285-74255263Ly4
SE_60464chr14:74207806-74255524DHL6
SE_61255chr14:74213654-74265085HBL1
SE_61792chr14:74207766-74255629Toledo
SE_62356chr14:74206365-74257143Tonsil
SE_65355chr14:74240820-74242152Pancreatic_islets
SE_65355chr14:74242412-74243379Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr147424169374241965
chr147424284474243173
Number: 3             
IDChromosomeStartEnd
GH14I073776chr147424250174242650
GH14I073775chr147424268174243090
GH14I073767chr147423430574242179
Enhancer Sequence
CCTCCACAGG TCTCTCTGAG TGGCACGCAG ACCTGGGATA ATGACAGGAA GCCTCTGAGT 60
GACAACCCTG GGTCCCACTA TGAGGCACCA TAAAGACACC GCCTGCCAGG CTCCATTCAC 120
AGGAATTTTC GAACAGGAAA GGTACCCCTG TAGTCTAATC CCCTCATTTC ATAGACAAAC 180
GGAGACTGCA ATCCCTGCTT TGGGGCTCCC ACTGCACCCT GCAATTACTG TCAGGAGGAT 240
GCATTCTTCC TCGCAGGAAC AGGAAGTGCC ACAGCCTGTC CTGACTGCCT CATGACCAGG 300
TGGGACAGGA CTTTCATTTT AAAGAGCCCC AGTCTCTGCT ACTATGGTCT GCAGACTTGC 360
TTTCCCCAGC TCTGTCTCTG TGTGAAGCCA AAAGACAGTG CTGAGCATGA GAAACGAAAG 420
GATCCTCTAA TGGCAGCTGG TATTAATATT TATCCTTCTT CAAGGAGGGC CAGTAGGAAG 480
AGATGCTTCT GCCACCTCTA AACCAGCTCC TCACCACAGA CATCTCCTCA GTGTCCCCTC 540
AAAGGCTTCC TCAGGGTGAG TGGGGCCCCG ATACAGGTTT TATACCCCCA AATCCCCTTC 600
CTACTCTCAC CAGGGTCTTG CTGACAGGCC CAAGCAAATA GCAGAGACAC CAAGGTGGCA 660
GCCCCACCAG CAAGCACTAA GGGAGGCTGG GGATGTCATG CAGACAGCCA GCTCACCAAG 720
CACACAGTCC ACCAGACATA GGCCAGGTCC TGGGCCTGCC CGATGCTCCC TCACAGCCCC 780
TCAGGTGGCC CTTCTCGTTC CTGTCACAGA GCACCTACTG TGTGCCAGCC ACAGATCCAA 840
GGTGGTGGGG AGCCAGGCAC TCCTGCAACT GACCCCAGCA TCCTGCAGGG GGGAAGTTCA 900
ATTGCAGAAA TGCCATGGTG GCAACTCAGG AAGGCAGCAT GGAGCAGGTG ACTCCTGGCT 960
GGCCCTGTGG GCATCTGCCA GGAGGAAAAG GCCAGAGAGG GCATTCCAGA TGGAAGAGAC 1020
AACAATAAGC AAAGGCCAAG AGCATATAAC AAGGCGAGAG AAGTGCGTCC AGGAGCAGCA 1080
AGAGGCCGGC TGGAACAAAA AGGGCCATGC TAGGGAAGGG GTAGTGGTAA GAAAAAGGCC 1140
AGAAAGGTGG GCCAGGGCTC AAACAAGAGT ACATGTGCCA TTCTGAGGAG TGTGGAGCTC 1200
CTTCTGCAGA ACTTGGGCAG TTCTCAAAGA TTAAGAGGGG GTGATATGAC CAAAGCTGTG 1260
TTTTAGTAAA ATAATTCAGG TTCTTCAAGA CTTCTTTTCC ACTTTAATGC TGCTTTTAGC 1320
ACAATTTCAT TTCATCTGGA CAAAAGTAGG CAAGTTCAGT GTAAACTAGG CCAGAACCAA 1380
CACTGGCCAG GAACTAGGAA GGCCCCTGCT CCCTCCCTCG GGGAGCCAAC CAGGCCATGC 1440
ATCTAAGCGA TCCAAGCCTC AGGATCAGGA ATCGCTTCCA GTCCAGAGCC CAGCTCATGA 1500
CACTCCCAGC TTCCTGGGGG CAGCAGCTTC CCGCTTTCCC AGGGAAGTCT TGGAACACTG 1560
GCATAAAACA GCCAGTAAGT TCAAAACTGC ATTTTTCCTT TTAAGGAAAA TTAATTCCTT 1620
TGTCTAAGAT TAATGGAACT GAATGACCAA GATTCCAGTC AAGGTGCCCT TGCTTCAAAG 1680
AGTTATACCC AGAAGATCTG AGGGCAAGAC GGGAGCTGGA GCTCACCTTA TCTGACACCT 1740
CTTGTTTTTT CTGGATGAGG AAACTGGGCA GGATGTGACA GGTGATGCTG ACAGCCCCAG 1800
GCAAACAAAG CTGTAGCTCC TTTAGCGCTC TCAGAAAGGA GATAGGGTAG AACATCTCAA 1860
CCAGGGTGAC ATCTTTAGAA CTGGAGAGAT CACCTGGGCA GCTTAGACAC CAGGCGCCTC 1920
AACTGTTCCA CAAACCAAGC CTGAAACCAG AACTCCAACT TCTAGTCTGA AAAGCAAAGT 1980
GGCACCTCGC AAACACCCTG TGGCCCCAAG AGTCTCACCC AACCTTGGGG AAGAAGCAGA 2040
ATTCAAGCTG TAACTGCCTG TTGGAGAGAG CCAACCCTCG GCCTCTGTCC TCGAAAGGCA 2100
GCACCAAAGT TTTCCAAGTG GAATCAAATG TGCAGGGAGG ATCCAGATGC CGGGATGATC 2160
TCCCTTTTCC ACTGGGATGG TCAGATTCCA GAGGAGAATT CCAATTACTA ATGAAACACT 2220
CAGATCTTCT GGGCACATAA CATTCCTAAA GCTCAGCGGG AGGCTAAGGA TTCAGAAGGA 2280
TGTCCAAACA GATTAAGCTC AAGATGTGGA TGTTGGCCAG GTATGGTGGC TCATGCCTGT 2340
CATCCCAACA TTTTGGGAGG CCAGGGTGGG AGGCTGGCTT AAGCCCGGGA ATTCAAGACC 2400
AGCCTGGGCA ACATGGCAAA ACCCCATCTC TGTTTAAATT ACAAAAAAAA AAAAAAAAAA 2460
GATGTGGATG TTTTCAGTGG CCCAAGAGGG ATGCCCTGTC TCCTCTTCCC ACATCCAGAA 2520
CAGCCCCATC ATCCCAGTTT GAAGGCTAGA ATGGGCTCCA AGCTCTATGA GAGACACCTG 2580
TCCACCTGGC ATATGCAGCC CTCCCCTGGT TTCAGGCACC TGTGGTTGTG AGTCCTGAGA 2640
GGAGGCAGAG TTCCACTCTG CTGGGGAGGC TGCAGCCTCC AGAGCCTTGC TCTTCAGAAC 2700
CGTAACATCA GCCTCAGGCT CACGCCTGTA ACCCCTGCAC TTTGGGAGGC CGAGGCGGGT 2760
GGATCACAAG 2770