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

TagContent
EnhancerAtlas ID
HS157-06416 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr17:79300980-79303940 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr17:79303447-79303458GGTGACTCATG+6.62
JUNDMA0491.1chr17:79303447-79303458GGTGACTCATG+6.02
KLF16MA0741.1chr17:79302493-79302504GGGGGCGGGGC-6.02
KLF5MA0599.1chr17:79302494-79302504GGGGCGGGGC-6.02
SP1MA0079.4chr17:79302492-79302507TGGGGGCGGGGCCTC-6.44
SP4MA0685.1chr17:79302490-79302507GGTGGGGGCGGGGCCTC-6.64
ZNF263MA0528.1chr17:79303272-79303293AGAGGAGGGAGGAGGGAGGAG+6.91
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_23211chr17:79302108-79305098Colon_Crypt_1
SE_26559chr17:79300946-79301389Esophagus
SE_26559chr17:79302232-79304772Esophagus
SE_27741chr17:79301633-79305758Fetal_Intestine
SE_28689chr17:79300868-79306340Fetal_Intestine_Large
SE_29929chr17:79301804-79304977Fetal_Muscle
SE_31718chr17:79302282-79304471Gastric
SE_34591chr17:79301530-79306049HCT-116
SE_35230chr17:79301694-79305379HeLa
SE_41800chr17:79301805-79304593LNCaP
SE_42641chr17:79300771-79301571Lung
SE_42641chr17:79301708-79305193Lung
SE_47367chr17:79301586-79304906Panc1
SE_48267chr17:79300913-79304968Psoas_Muscle
SE_49267chr17:79300756-79301454Right_Atrium
SE_49267chr17:79302245-79304134Right_Atrium
SE_50704chr17:79300768-79301473Sigmoid_Colon
SE_50704chr17:79302148-79304837Sigmoid_Colon
SE_52831chr17:79300804-79301493Small_Intestine
SE_52831chr17:79302321-79305169Small_Intestine
SE_53485chr17:79300595-79301475Spleen
SE_53485chr17:79302655-79304056Spleen
SE_56913chr17:79302223-79303451VACO_400
SE_56913chr17:79303471-79305245VACO_400
SE_57608chr17:79301790-79305121VACO_503
SE_58079chr17:79301741-79305485VACO_9m
SE_65666chr17:79301842-79305088Pancreatic_islets
SE_69098chr17:79301779-79304921H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177930176479301840
chr177930197479302367
Enhancer Sequence
GACCCCAAAT CTTCTGTCTG TCTTTGTGAA TGGCCTGTTC TAGAAGTTGC ACAGAAGTGG 60
AAGCACACAC CACGTCCCTT TCTGTCTGGA ATTCCTCAGT TAGCATAACG TCCCTGAGGT 120
CCATCCACGC AGTAGCGGGT GTCAGATTTC CTTCCTTTTC CAGGCTGAAC CCTGTTCCAC 180
ACGTGGCTAG ACCACAACTT GTGTGTCTGT CCACTCATGG GTCGACGGCA CTTGGGTGCT 240
TCCACCTCCT GCTGGCCGTG ACCAGGGCTG CTGTGGACTC TGGCGCTCTC GTCTGCACCA 300
GCTGCTGCCT TCAGTTCTCT GGGGTCTGTA GCCGGAGTGG CATCGTTGAG TCACGTGGGA 360
ATCCTGTGCT CTGCTTTTTT TCTTTTCTTT TCTTTTCTTT TTTCTTTTCT TCTTTTCTTG 420
AGACAGAGTC TTGCTCTCTC ACCCAGGCTG GAGTGCAGTG GTGCGATCTT GGCTCCCTGC 480
AACCTCCACC TCCCGGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGATT 540
ACAGGTGTTC ACCACCACGC CTGGCTAACT TTTGTCTTTT TAGTGGAGAT GGGGTTTCAC 600
CATGTTGGCC AGGCTGGTCT CAAACTTCTG ACCTCAGGTG ATCCGCCCAC CTTGACCTCC 660
CAAAGTGCTG GCGTTACAGG CGTGAGCCAC CGCACCCGGC CTATGCTCCA CTTTTTGAGA 720
GGCCAACAAA CCCCACTTGC TTTTTCAATC CAGATTTTAA CCTTTGAGGG AAAAGAAAGA 780
TTTTTGTATC TATTCCTGGG CCGGGGTAGG GGGGCTGTTG GGTGAGGAAC ACCCAAGAAC 840
GGCTCAGGTG AGAGGGGTGG CCTCTAAGAC CACATGGCCT GGACACAGCC TGGCAGGCAG 900
ACCGAAGCAG CCGGGGCTGC CTGGAGGGCC TCAGTTCTGC TCCTCCCCAG CTGCAGGATC 960
TGAGCAGGAG GCCTCCTCAC TCTGCGCCTC AGTTTCCTCA TCTTTATCTG GGGACGGAGC 1020
AGCCTCTACC TCTCAGAGCT AGTTGCGATC ATGGTGGCAG CTGAGGCCCA GCCCTGGTAT 1080
GCAGTGAGGG TTCAACTGAG CCAGCCCCCA CTCGCCACAG GCTTGCCTGG GGAAGACAGG 1140
TGCATCAGCC CCGGGGTCCA TTTCGCAGTG GGGCTGATCC CAGCCCACCC TCACCCGCCC 1200
GGGAGCCTCG CCCTTCACCC CATGCATCTT CTCCCCTGAA TCACCCCCAG GGTCTCCAGG 1260
GCAGGAGCAG GGCTGGCAAG GGCAGGGCTC ACAGCCCCAT AGGGAGGACA CAGTGCCCGC 1320
AAGAGGGACT GGGCAAGAGG TGGACAGGCA GGGGGTGGGG GCATTCTGTG TGCCCCAGAG 1380
CCTGAGTTCG CAGGCTCTCA GCAGCCCGTG CTGGGCAGCA GTGTGGGCGT CTCTCCCGCA 1440
GGGCACCCTC TGCACTTTCC TGCAGACCTG CAGCAGCCCT TTCCTGAGGG ACACCTGGCT 1500
CCGGGCCCAG GGTGGGGGCG GGGCCTCGCG TGTCTCCCCC TTGATTTGTA AGAGTCCAGG 1560
GCTGTCGGCC ATGGCCACAC TGAGCACCCC TGGGAGCCAA GGCAGCTTAA GGACAAGGTG 1620
TGTATGAGGA CGGCGGGGCC CAGGGAGGAG AGGCTAGCCC AGGGCTACCC GGGTCCCCGG 1680
AGTAGGGGCA GGGGACTTGA AAATGAGCCC CCAAGGGGCT CTGATGGGGG CAATTCCAGG 1740
AGAGGCGTGG GCAGGTGTGG GGCTGGAGAG AGGCCTGTCC TTTTTCCCTT GCCCTGCACA 1800
CTGTCTGCAG GGTGGCAGAC CCAGGCTGCC TGGCGAGGCT GCTTCTGGAG GCCTGAGGAA 1860
GGCTGGGCTG AGGACTCCGC CTCTCCTCAA AGCCACAGCC TCCCTGCTCT GGGGCTACAT 1920
GTCGGGAAAA TCCCTGCCTG GGTTACCCCA GCTGGGGACT CAAGCTCTCT TTGGACCCTA 1980
CAGAAAGAGC TGGCCAGCCC CCAGGCCAGA AGGGCCGTCC GTGACCCACA GATGGCCCCA 2040
ACACACTGTA AAACACGCAT GATTTATTTT AGTGTGTGTT AGAAAAATAA AGCCAACACA 2100
TCAAGCCTGC AATTTCGCAG ATACTAACAC TTCGGACCAG GAAAAAAGAA GCCCATGACA 2160
TGGCACAGCG CTGTGGAGCG AGCGAGATCT GGGATGCGTA GGCCTGGACG GCTGAGGCTT 2220
GGAAACCCCT CCCCTCCCCA AACTTTCCCA CCATGCAGGG GCCCAGCAGG CCCTCAGCCC 2280
ACTCACCCCG CCAGAGGAGG GAGGAGGGAG GAGGGTCCGG GCCAGGTGGG AGCTTCTCCC 2340
CGGAGGCCTG AGGCAGCTTC CCTCCTCTCC CAGGAAGGGG CTGGCCCAGG CCCAGCTAGG 2400
ATGCTCCCAG CCCAGCTCCT ACCCGCCGGG TCTTTCCCGT TTGTCAGGCA GGCCGGCAGG 2460
CTGGGCTGGT GACTCATGAC TGGCTGGGCC ATCTGCCCTG CACCCCTGCC CCGGGCGAAG 2520
TGAGAAACCT GACCGGGCTC CAGCACAGAC AGGAAACCCC ACCCCAGGGC CTGCAGTGGG 2580
ACAGGTGTGG CCGCCCTCCA CCCCCACACA GGCCTCGGGG AGGGTGTCTG AGGCCGGCCT 2640
GGCCCTCTCT GCAGCACTGA AACACCAGCT GCCTCTCCCC AGCCCGGAAC TGGGGATCCA 2700
GTGTCCTCCG CACTGACCCC AGGCTCTGCT CTCCCTGGGA AGCACCCGCT TTGACAGTGG 2760
GGCCAAGGAC TGGGGTTCCC ACCCTCCTCT GCCCAGTGGA CTTTGTGGCC CCAGGCAGGT 2820
GGCATCAGCT CTCTGGGCCT AAGCTTCTCA TCTCTGCAGG GTTCATCAGC TCAACAAGCA 2880
TTTGTGGGTT CCTGAGACCT GAAGGCTCCA CTCCCCCACC TAAGCACACA ACAGTCCAGG 2940
CACCACCCAC ATCTCCCTCT 2960