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

TagContent
EnhancerAtlas ID
HS183-02552 
Organism
Homo sapiens 
Tissue/cell
T47D-MTVL 
Coordinate
chr17:79301070-79303940 
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
ATTCCTCAGT TAGCATAACG TCCCTGAGGT CCATCCACGC AGTAGCGGGT GTCAGATTTC 60
CTTCCTTTTC CAGGCTGAAC CCTGTTCCAC ACGTGGCTAG ACCACAACTT GTGTGTCTGT 120
CCACTCATGG GTCGACGGCA CTTGGGTGCT TCCACCTCCT GCTGGCCGTG ACCAGGGCTG 180
CTGTGGACTC TGGCGCTCTC GTCTGCACCA GCTGCTGCCT TCAGTTCTCT GGGGTCTGTA 240
GCCGGAGTGG CATCGTTGAG TCACGTGGGA ATCCTGTGCT CTGCTTTTTT TCTTTTCTTT 300
TCTTTTCTTT TTTCTTTTCT TCTTTTCTTG AGACAGAGTC TTGCTCTCTC ACCCAGGCTG 360
GAGTGCAGTG GTGCGATCTT GGCTCCCTGC AACCTCCACC TCCCGGGTTC AAGCGATTCT 420
CCTGCCTCAG CCTCCCAAGT AGCTGGGATT ACAGGTGTTC ACCACCACGC CTGGCTAACT 480
TTTGTCTTTT TAGTGGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CAAACTTCTG 540
ACCTCAGGTG ATCCGCCCAC CTTGACCTCC CAAAGTGCTG GCGTTACAGG CGTGAGCCAC 600
CGCACCCGGC CTATGCTCCA CTTTTTGAGA GGCCAACAAA CCCCACTTGC TTTTTCAATC 660
CAGATTTTAA CCTTTGAGGG AAAAGAAAGA TTTTTGTATC TATTCCTGGG CCGGGGTAGG 720
GGGGCTGTTG GGTGAGGAAC ACCCAAGAAC GGCTCAGGTG AGAGGGGTGG CCTCTAAGAC 780
CACATGGCCT GGACACAGCC TGGCAGGCAG ACCGAAGCAG CCGGGGCTGC CTGGAGGGCC 840
TCAGTTCTGC TCCTCCCCAG CTGCAGGATC TGAGCAGGAG GCCTCCTCAC TCTGCGCCTC 900
AGTTTCCTCA TCTTTATCTG GGGACGGAGC AGCCTCTACC TCTCAGAGCT AGTTGCGATC 960
ATGGTGGCAG CTGAGGCCCA GCCCTGGTAT GCAGTGAGGG TTCAACTGAG CCAGCCCCCA 1020
CTCGCCACAG GCTTGCCTGG GGAAGACAGG TGCATCAGCC CCGGGGTCCA TTTCGCAGTG 1080
GGGCTGATCC CAGCCCACCC TCACCCGCCC GGGAGCCTCG CCCTTCACCC CATGCATCTT 1140
CTCCCCTGAA TCACCCCCAG GGTCTCCAGG GCAGGAGCAG GGCTGGCAAG GGCAGGGCTC 1200
ACAGCCCCAT AGGGAGGACA CAGTGCCCGC AAGAGGGACT GGGCAAGAGG TGGACAGGCA 1260
GGGGGTGGGG GCATTCTGTG TGCCCCAGAG CCTGAGTTCG CAGGCTCTCA GCAGCCCGTG 1320
CTGGGCAGCA GTGTGGGCGT CTCTCCCGCA GGGCACCCTC TGCACTTTCC TGCAGACCTG 1380
CAGCAGCCCT TTCCTGAGGG ACACCTGGCT CCGGGCCCAG GGTGGGGGCG GGGCCTCGCG 1440
TGTCTCCCCC TTGATTTGTA AGAGTCCAGG GCTGTCGGCC ATGGCCACAC TGAGCACCCC 1500
TGGGAGCCAA GGCAGCTTAA GGACAAGGTG TGTATGAGGA CGGCGGGGCC CAGGGAGGAG 1560
AGGCTAGCCC AGGGCTACCC GGGTCCCCGG AGTAGGGGCA GGGGACTTGA AAATGAGCCC 1620
CCAAGGGGCT CTGATGGGGG CAATTCCAGG AGAGGCGTGG GCAGGTGTGG GGCTGGAGAG 1680
AGGCCTGTCC TTTTTCCCTT GCCCTGCACA CTGTCTGCAG GGTGGCAGAC CCAGGCTGCC 1740
TGGCGAGGCT GCTTCTGGAG GCCTGAGGAA GGCTGGGCTG AGGACTCCGC CTCTCCTCAA 1800
AGCCACAGCC TCCCTGCTCT GGGGCTACAT GTCGGGAAAA TCCCTGCCTG GGTTACCCCA 1860
GCTGGGGACT CAAGCTCTCT TTGGACCCTA CAGAAAGAGC TGGCCAGCCC CCAGGCCAGA 1920
AGGGCCGTCC GTGACCCACA GATGGCCCCA ACACACTGTA AAACACGCAT GATTTATTTT 1980
AGTGTGTGTT AGAAAAATAA AGCCAACACA TCAAGCCTGC AATTTCGCAG ATACTAACAC 2040
TTCGGACCAG GAAAAAAGAA GCCCATGACA TGGCACAGCG CTGTGGAGCG AGCGAGATCT 2100
GGGATGCGTA GGCCTGGACG GCTGAGGCTT GGAAACCCCT CCCCTCCCCA AACTTTCCCA 2160
CCATGCAGGG GCCCAGCAGG CCCTCAGCCC ACTCACCCCG CCAGAGGAGG GAGGAGGGAG 2220
GAGGGTCCGG GCCAGGTGGG AGCTTCTCCC CGGAGGCCTG AGGCAGCTTC CCTCCTCTCC 2280
CAGGAAGGGG CTGGCCCAGG CCCAGCTAGG ATGCTCCCAG CCCAGCTCCT ACCCGCCGGG 2340
TCTTTCCCGT TTGTCAGGCA GGCCGGCAGG CTGGGCTGGT GACTCATGAC TGGCTGGGCC 2400
ATCTGCCCTG CACCCCTGCC CCGGGCGAAG TGAGAAACCT GACCGGGCTC CAGCACAGAC 2460
AGGAAACCCC ACCCCAGGGC CTGCAGTGGG ACAGGTGTGG CCGCCCTCCA CCCCCACACA 2520
GGCCTCGGGG AGGGTGTCTG AGGCCGGCCT GGCCCTCTCT GCAGCACTGA AACACCAGCT 2580
GCCTCTCCCC AGCCCGGAAC TGGGGATCCA GTGTCCTCCG CACTGACCCC AGGCTCTGCT 2640
CTCCCTGGGA AGCACCCGCT TTGACAGTGG GGCCAAGGAC TGGGGTTCCC ACCCTCCTCT 2700
GCCCAGTGGA CTTTGTGGCC CCAGGCAGGT GGCATCAGCT CTCTGGGCCT AAGCTTCTCA 2760
TCTCTGCAGG GTTCATCAGC TCAACAAGCA TTTGTGGGTT CCTGAGACCT GAAGGCTCCA 2820
CTCCCCCACC TAAGCACACA ACAGTCCAGG CACCACCCAC ATCTCCCTCT 2870