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

TagContent
EnhancerAtlas ID
HS034-13392 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr17:79318860-79320670 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr17:79320162-79320176CAGGGGGCGTGGCT-6.17
KLF16MA0741.1chr17:79319886-79319897GCCCCGCCCCC+6.02
KLF16MA0741.1chr17:79319900-79319911GCCCCGCCCCC+6.02
KLF16MA0741.1chr17:79320164-79320175GGGGGCGTGGC-6.62
KLF5MA0599.1chr17:79319886-79319896GCCCCGCCCC+6.02
KLF5MA0599.1chr17:79319900-79319910GCCCCGCCCC+6.02
SP1MA0079.4chr17:79320163-79320178AGGGGGCGTGGCTGG-6.31
SP3MA0746.2chr17:79320163-79320176AGGGGGCGTGGCT-6.46
SP4MA0685.1chr17:79320161-79320178CCAGGGGGCGTGGCTGG-6.14
SP8MA0747.1chr17:79320163-79320175AGGGGGCGTGGC-6.92
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_23211chr17:79314291-79319887Colon_Crypt_1
SE_23211chr17:79320130-79320935Colon_Crypt_1
SE_24639chr17:79317732-79319905Colon_Crypt_2
SE_24639chr17:79320175-79320792Colon_Crypt_2
SE_26559chr17:79314278-79320927Esophagus
SE_27741chr17:79309202-79319885Fetal_Intestine
SE_27741chr17:79320070-79320959Fetal_Intestine
SE_28689chr17:79309121-79319983Fetal_Intestine_Large
SE_28689chr17:79320119-79321007Fetal_Intestine_Large
SE_29929chr17:79314211-79319932Fetal_Muscle
SE_29929chr17:79320117-79321126Fetal_Muscle
SE_31718chr17:79314230-79321845Gastric
SE_35230chr17:79316272-79319932HeLa
SE_41800chr17:79317801-79319996LNCaP
SE_41800chr17:79320153-79321041LNCaP
SE_42641chr17:79314293-79320047Lung
SE_42641chr17:79320062-79321138Lung
SE_47367chr17:79311638-79319848Panc1
SE_47367chr17:79320101-79321519Panc1
SE_47524chr17:79316349-79319991Pancreas
SE_47524chr17:79320113-79320944Pancreas
SE_48267chr17:79312119-79321146Psoas_Muscle
SE_49267chr17:79314350-79320037Right_Atrium
SE_49267chr17:79320068-79321472Right_Atrium
SE_50704chr17:79314343-79319977Sigmoid_Colon
SE_50704chr17:79320065-79320981Sigmoid_Colon
SE_52831chr17:79311991-79320037Small_Intestine
SE_52831chr17:79320064-79320863Small_Intestine
SE_53485chr17:79310100-79320902Spleen
SE_56913chr17:79316324-79319872VACO_400
SE_56913chr17:79320129-79321047VACO_400
SE_57608chr17:79316317-79320037VACO_503
SE_57608chr17:79320167-79320769VACO_503
SE_58079chr17:79316241-79319859VACO_9m
SE_58079chr17:79320164-79320688VACO_9m
SE_65666chr17:79312097-79319865Pancreatic_islets
SE_65666chr17:79320107-79321062Pancreatic_islets
SE_68308chr17:79314112-79339705TC32
SE_68600chr17:79315119-79324556TC71
SE_69098chr17:79316259-79319952H9
SE_69098chr17:79320178-79320888H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177931981279320225
chr177931932579319648
Enhancer Sequence
GCCTCCTCGG ACCCCGCAGA ATACCCCCAA AGCCCATGGG CGTCTCCTAA CCGTGTAAGT 60
CCGGGGCTCC GGGGGCTAGG AGGGGCTGCT CCAAGACAAG GGAAGCTGCC CGCCAGATTG 120
GGGCCAATAT CGGGCTTTCC CAACCCAAGC TTCCTCCGAA AACAACCCCC TCAAAACTGA 180
GCATCCCTAC TAGAAAAAAT CCGCATTTTC CAGGAGGACG GGGTGGGAGA GCTTCGGGGA 240
ACAAAGCCCG GTCCTCCCAG CTCTGAGGCC GAGGCAGGGC GCACCTCCTC CTGGGCGAAT 300
TCAATCGGAG CTGCAGAAGA GACAAGCATT TCCAAACTGG CACCCGCTCC GAGCCCAAGG 360
TGAGGGTGGA GAAGGGTCCC TGGTGGAAGC TGCAGGAACA CTTTGGGCCG GGGTCTACCC 420
CGCGTTCGGC GGCTCCCCGA ATCCCGCAGA AAGACACGTT TGCAGCGAAA GGCTCTTACA 480
CACCAGCCGG GATTTTATTC GTTCCCTACC GAGAGTGCGC TCTGGGAGCG CGGGAAACAA 540
GGAAAACGCA CGTACCTGGC GGCGCTCCGA GGGCGGCCTC GCGGGCCCTC CGCTGGCGAA 600
GGCCCCCAGA AGCCACTCCC CGCCCGGCTG CTCGCCCCAC GGCCAGTCCC TCCCTCCCCG 660
GCGACGCACC CCGCCGAGCC AGCTCACAGG AAGCGCCAGG AGCCGGAGAC CTGGCTCGCC 720
TTTCCGGGCG CTGCGTCCGT CTTCGACCGC CAGGGCCCGC GTCCTCTCCC CGGCCACGGC 780
CCACCAGAGG GACCCCGCGG CGGGTCCTGG CTCGGGCGCG TCCTTCTGCG TCCGAGTTCC 840
CAGGTTCCCG GCCGAGCTGC GGAGACGGAC GCGGAGCCCT CGGGGAAGAC GAGGCGGCGG 900
CGGCCGCCGT CCGGGCAGGA GCCCCGGGGC GGGAGGGGTG CAGGGCGGAG GAGCGGGCGG 960
GATCCCAGCG CCCCGCGCCC CGCGGCCGCC GCCCTCCGGG GCGCCCAGCC CCACCCACGT 1020
GGAACCGCCC CGCCCCCGCC GCCCCGCCCC CACGAGGGAA GGCACCCGAG CCTCGCCGCA 1080
CACCCGCGCC TCCCGGTCCC GGGCCCGAAA CACCGCGCCC CTCCCCCAGC GCCGTGCTCC 1140
CCGCCTCTCC AGCGCGCGGC TCCCGCCCGA CCCGCGCGCC CGCCCGACCC GCCCCCAACC 1200
CCGCCCAATC ACCGCCCTCC GCGGCTGCTC CCTTTGTCTG AGCCCCCGGC GCAGGCCAAT 1260
GGAATCACGC GGAGGCGCGG GCGGCTTGGC CAATGGAAGG CCCAGGGGGC GTGGCTGGCG 1320
GGAGGGGCTG CGGGCGGCCG GGTTCTATGC GCTGAGACCC GAGACTGCGT CGCCGGCGGG 1380
TGCGCCCAGG TCGCCCAGCT AGAGCCGGCA GGATCCCGCC GCCGGGTTGT GGGTTTTTGA 1440
CTCTCCCTCC GCTGTCGGGA GAAGCGCCTG AGTGGGGAGG GAGGTGGGAG GAGGTGGCCC 1500
CGCGTCGGGG GTGCGGGGAG CGGGACGGCG GCTTGGATGG ACACGGTCAG CCCCGGGCCG 1560
GAGAGGGTTC GGCTCAGAGC AGCCTGGGTT CTGTTCAGAG CCCTACTGTG CACGTTTCCG 1620
CGAGGATCTG CGGAGAGACG TGCAGGCGAC GCAGGCCCCG GGAAGGAAGG AGGGTACCTG 1680
GGCTCGGACG AGCGATAACG CTGTGTTCTG TGACTCCGTA CAAACGGATC CTGGAGTCCA 1740
GGGAAAGCGT CCCAGGCCCC CAGCCCGGGC AGGGTTCGTG GGATTGGCGT CCGCTGCCCC 1800
AGGCTTACCC 1810