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

TagContent
EnhancerAtlas ID
HS091-33050 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr22:36865300-36868000 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr22:36866464-36866483TGGTGCCCTCTAGTGGTCT-7.42
LMX1BMA0703.2chr22:36866575-36866586TTAATTAAAAT-6.62
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01080chr22:36865998-36866589Adrenal_Gland
SE_01080chr22:36866604-36869281Adrenal_Gland
SE_01722chr22:36859233-36865838Aorta
SE_01722chr22:36865877-36869195Aorta
SE_02575chr22:36865950-36867881Astrocytes
SE_23071chr22:36865956-36866534Colon_Crypt_1
SE_26443chr22:36864997-36869260Duodenum_Smooth_Muscle
SE_27096chr22:36864934-36865828Esophagus
SE_27096chr22:36865885-36869301Esophagus
SE_27650chr22:36865840-36866663Fetal_Intestine
SE_27650chr22:36867046-36867861Fetal_Intestine
SE_31378chr22:36865090-36865830Gastric
SE_31378chr22:36865922-36867714Gastric
SE_37504chr22:36860602-36869250HSMMtube
SE_41064chr22:36865109-36865869Left_Ventricle
SE_41064chr22:36865943-36866692Left_Ventricle
SE_42094chr22:36865103-36865854Lung
SE_42094chr22:36865903-36867855Lung
SE_46578chr22:36865089-36869239Osteoblasts
SE_49127chr22:36865124-36865756Right_Atrium
SE_50050chr22:36865120-36865825Sigmoid_Colon
SE_50050chr22:36865899-36867851Sigmoid_Colon
SE_51467chr22:36865103-36866710Skeletal_Muscle
SE_51467chr22:36867277-36868112Skeletal_Muscle
SE_52340chr22:36865118-36866653Small_Intestine
SE_52340chr22:36866655-36867858Small_Intestine
SE_53283chr22:36865879-36868971Spleen
SE_54687chr22:36859233-36871332Stomach_Smooth_Muscle
SE_55607chr22:36866484-36867685Thymus
SE_63127chr22:36801020-36866853Tonsil
SE_64152chr22:36865109-36869139HSMM
SE_65459chr22:36865826-36866909Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223686606736866406
chr223686603336867878
Number: 1             
IDChromosomeStartEnd
GH22I036457chr223685347536869221
Enhancer Sequence
CAGCGCCCGG CAAATAAGCT TAGGAACCTG GCATTGTGCC TGGCATACTG TGGGCATTCA 60
AAAAACAGTG GCTACAGAGG GCACAAGGAA AAGTCCAACA CAGGCCCCAC GAGAGCACAT 120
TAGCTTGCTG CTGTGATGAG TGACAGGGTC CAGAAACTCA GGGACTTCTA CTGGACAGCA 180
TGAGAGGAGA GGCTTGGCCA TACACAACCT GACGCTTATT AGCAGGTTGC AGGCAGATGG 240
CAAGGACAAC ATTCTTGGTC TGTGAAGCAT TTACTCAGTT CCCTCAGGGA CCTGCATAGG 300
TTATGTGGAA CGTGGATGAG GCTGTGGCCC ACCAGACTGG CATTGTGAGG TCTCTGCTGC 360
CTGGGATCCC TGCCTGGCAT TCGTGGGCAT TTGAGAAAAC CATTTAAACA GAACAAGATA 420
GGCCGGTCGC TGTGGCTCAC GCCTGTAATC CTAGCATTTT GGGAAGCCAA AGCGGGCAGA 480
TCACTTGAGG TCAGGAGTTC GAGACCAGCC TGACCAACAT GGTGAAACCC CGTCTCTACT 540
AAAAATACAA AAATTAGCCG GGCGTGGTGG GGCATGCCTA TAGTCCCAGC TACTCGGGAG 600
GCTGAGGCAG GAGAATCGCT TGAACCCGGG AGGCAGAGGT TGCACTGAGC TGAGATTGTG 660
CCATTGCATT CCAGCCTGGG CGACAGAGCA AGACTCTGTT CCCCCCCTCA AAATAAATAA 720
ATAAAAATAA ACAGAACAAG ATAAACACAG ACTTTTCTTA CATACAAATT AAACTACAAA 780
GTAAGAGCAG AGATTCACAC AAACATACCA GGTCTTCACA TATCCCAGTG CTGCCCTGCC 840
ACGGCCCATC TTGGAAGCCA GTAAGATTCA GAATGTTCAA AAACCATGCA CATGGTAGTT 900
AGGAAAGGCA CGCAGGCCAG ACCATCCCGC CCTCACCCAC TAACTTTACG TGGCAGGCCC 960
TGCACCCCAC TCCTCACGGA CACTTTGGGG ACAAACACAG CAGGTCACAG GACACAGTCC 1020
TTGTCCTTGT TAGTGCCTCA GGCCCCTTCA AAGGCTGTCC CTGGGCTGAT GTGGGTGGCA 1080
AACCCTGTCT CCAGGCAGAG CAGGGCCCGA AAGAGTTTGC TCCAGGAAGC GCCTGAAGCC 1140
ACCAGGGCCT TCCCAGGCAT TCTTTGGTGC CCTCTAGTGG TCTGCAAAGG CAGCTGGAGT 1200
GCCTCAAAGC CGGAGCCTCT TGGCAGAAGC AGAGAGCTCA GCCACCGGCT CCCACCTGCA 1260
CACTGTCCTA TTCCTTTAAT TAAAATATAT GCTTTATGCC ACTGTATAAG AAGTGGCCTA 1320
ACTTTTTTCA CGGCAAGACT CTAAGTTCAC TGAAGAGGCT CAGAGAGTGG ACTTAGCGTT 1380
CCTTAAGAAC TCCAGATAGG CACAAGCACA GTGGCTCACA CCTGTAATCC CAAGTACTTT 1440
GGGAGGCCAA GGCAGGAGGA CTGCTTGAGG TCAGGAATTC ATGACCAGCC TGGGCAACAT 1500
AGCAAGACGT CGTCTCCATA AAAATATTAA AAAAAAAAAA AAAGAACTCC AGATGAAGGC 1560
CATAATGATC TCACTCATGT AAACCTCCAC ACATGCTTGA ACACGCACAG ACCCTGCTGG 1620
TGTCAGGTAG ACAGCAGATG TGCTGTCAAT GGAGGTCTGG TCACTACTGA TCAAGGGGAT 1680
ATTTTGAAGT TGAGCTTAAA CACACACACG CATACACACA TATATACACA CACACACATA 1740
CACACTACCC GCACTAGGGG CTCACAGGAA ACCTGAGCTG GAATGGGACT TCCCTCGACC 1800
CTGAGGAGGC GGCTGAAGCT CTGCTGCTCC TGTGTCTGGC TCACACATCA GGAGGTGCCG 1860
GTGCCTGTAA ACACTGCCTT ACATGGAAGT GCACAGGGCC TTGGCACATT CTTCTGGAAT 1920
GTTTTGAGTG TGAAAGAGGC AGTGACTGAG CCAACTGAGG GGCTGAGGAA AAGATACGCT 1980
ACGACGTGTT GCCTGTCCTG TTCCGTGAAG CCACTTGGAA CCTCCTATCC TTGGATAAAG 2040
ACCCTCTGAA CTCGGCAGGA GTGGGGGAGT GTGTACGTGT GCGCAGTCTC TTTCTGCTAA 2100
CCCGTAGCTC GCCTGCACCG CCACTGAGCT CCGTGTCCTG GTATGTCTTC TCCTGTCCCA 2160
CCCCGATGGC ATCCATCTGT TAACTCAGCT AAGGGCCTAC CAAGGGAAAG GCACAGTGCT 2220
GGGTGCTGCG GGATGTTGCA ACCTCCTCCT CGGCTCATTG CAGAGTTAAA AGGAAAAGAT 2280
CGCTGTCACA TGCTGGGTGC TTTTTCGTGT CAGGAATGAT ATAAACACCT CTATACACTA 2340
TCTCACACTC TCCTGGCTGT GGGCAGGATC ATTTTAACGA TGAGAATACT GAGGCTCAAA 2400
GGGTGAGCAA CTGTTCCAAA ATGATGTGGT GTAGGACAGG CGCGGCAGCT CCTGCCTGTA 2460
ATCCCAGCAC TTTGGGAGGC TGAGGAAGGT GAATCATCTG AGGTCAGGAA TTCGAGACAA 2520
GGCCGGCCAA TGTGGTGAAA CCTTGTCTCT ACCAAAAATA CAAAAATTAG GCCGGGCGTG 2580
GTGGCTCACG CCTGTAATTC CAGCACTTTG GGAGGCTGAG GCAGGAGAAG TGCTTGAATG 2640
CGGGAGATGG AGGTCGCAGT GAGCCGAGAT TGCGCCACTT CACTCCACCT GGGTGAAAAG 2700