EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-12580 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr14:100037730-100040370 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CENPBMA0637.1chr14:100039543-100039558CCCGCCTAGAGCGAA+6.27
KLF4MA0039.3chr14:100040254-100040265CCACACCCTCC+6.32
SCRT1MA0743.1chr14:100039174-100039189GTGCAACAGGTGCTC+6.69
SCRT2MA0744.1chr14:100039174-100039187GTGCAACAGGTGC+6.98
ZEB1MA0103.3chr14:100038184-100038195CCCACCTGCCC+6.14
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00922chr14:100035637-100043899Adrenal_Gland
SE_06477chr14:100038631-100041912Brain_Hippocampus_Middle
SE_23140chr14:100036955-100039552Colon_Crypt_1
SE_23807chr14:100037637-100039039Colon_Crypt_2
SE_23807chr14:100039076-100039579Colon_Crypt_2
SE_24879chr14:100037657-100039003Colon_Crypt_3
SE_24879chr14:100039033-100039685Colon_Crypt_3
SE_24879chr14:100039766-100043514Colon_Crypt_3
SE_26586chr14:100036268-100048060Esophagus
SE_27780chr14:100036471-100039970Fetal_Intestine
SE_27780chr14:100039991-100043446Fetal_Intestine
SE_28740chr14:100028345-100039820Fetal_Intestine_Large
SE_28740chr14:100039953-100043495Fetal_Intestine_Large
SE_31455chr14:100036155-100044158Gastric
SE_40985chr14:100034161-100047061Left_Ventricle
SE_41558chr14:100034157-100047015LNCaP
SE_42529chr14:100036484-100047048Lung
SE_47508chr14:100038066-100043477Pancreas
SE_49276chr14:100037919-100046958Right_Atrium
SE_50321chr14:100037583-100043539Sigmoid_Colon
SE_52517chr14:100037952-100043555Small_Intestine
SE_54552chr14:100023051-100046861Stomach_Smooth_Muscle
SE_57311chr14:100039853-100043812VACO_400
SE_61471chr14:100013991-100069569Toledo
SE_65289chr14:100029330-100043813Pancreatic_islets
SE_68735chr14:100036287-100038750H9
SE_68735chr14:100039105-100043753H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr14100037991100038153
chr14100038183100038299
chr14100038396100038481
Number: 1             
IDChromosomeStartEnd
GH14I099560chr14100026360100044326
Enhancer Sequence
CCAGCTCCAG CTGCTGTGAT GACCAAGTGC CTTTTGGGCG TGCAGGTGCC AGAGGTGCAC 60
AGCCGTGCCG TTCTGTAGGC CCCACTGGAA GGCTGAGACG CAGACCAAAG GCCCACAGGC 120
AGCAGCACTG GGCTACCCTG ACGGGGAGGT TCAGCCACGT CTGCAGGGGA GCAGGCGGGC 180
CCCTCCACCA CTGGAAAGAT CAAACACAGT CATGGATGTT AAATGTGCTT TGTAGAATCT 240
CAGATTCTTT TCTTCCCCAC TGTTTGCAGT AAGATTTACG ATGCCAGCAA CTCCTTAGAG 300
AAAAAAAGTG GCTGGGAAAT GGAATCACAT GCACAGGGTA ATTTGTGGCC TGTCCGGGCC 360
TTTGCCAATG TAAATATTTC AGGCAGGTAG GTGCCCAGTT CAATGCCCCC TGTGACAAGA 420
GCCTGTCTCC AGTGAGCTGA TCAGAACAAC AAATCCCACC TGCCCCTTTT CTTCCTGCTT 480
TCTGGCACCT CTTGGCACAT GGGTGGCCTG GGACATCACA CCTATCCAGC CTCCTGCCTC 540
ATTGAGCTAG GCCCTGAAGC CTCAGGGGAA GGAACTGGAG GGGACAAGGA GTGAGGCATG 600
TGGGCCAAGG AGCTGGAGAC TGCCTGCAGC AGGCACCCTT CCACGGGGCA TCTCAGAGCG 660
TGATCCCCAG AGCCCCCAAC CCTAACCCAG CACCCGCAAG TCTCTGGAAG GCAGCGGCAA 720
GGGCCAGATT CCCCACATAC CCTCCCAAGC CTGAGGGCTC AAATTCACAG GGTGGTGGTC 780
CCTAGAAAGA CCTCCAGGGT GGGCTTCAGT GGCCCTGGCC CCAGCAGCGT TAGTGAATGG 840
CCAGGCTGTG GCCCTCCCCG AGAGTCCCTC CCTCCCCAGG GATGGGTCTT TTCATGCCAT 900
CACTGCCGTC TCCTCCCCGC TACTTTCCCC AAGGAAACTG AAAGCTGTGG CATGTGGCCT 960
TCCTCACGGG ACACTGCGGG CGCTGCGGGC TAGTGTCTCA GCCTGCAATC CCGGCTCCCA 1020
CCCCCACCCC AAGGCCCTGC TCCACAGGGA AGCCAGAGGG CCTCACAAGT ATAAATGATC 1080
AGGTATCACA CCTCCGCCAG GCTTTAGATA AAATCCCAAC CCCAATAGCT CCTCCTACCC 1140
TGCCCCCTTC GGTCACCAGA GTCCAGCCAC AGGGCCTGGT CAGCTCCGGG AAAGCTCTGA 1200
CATCTGTCCT TTGCTGGAAA CCTTCCAGGG ACGACAGCTG CTTATCATCC AAGCCCCAGG 1260
TGACCTGGCC CCTCCTTAAG AGGCCTCCCC TGCCACCATC TGTTTTCTGC TCTTCCTAGC 1320
ACTCACCAGG ATATGAAACT GTCCCATCCA TGGATTTGTT TGCCAGTTTA TCCATCTTCC 1380
AAAGGAGACT TCTGTCTGTC TTGCTTCATG GAAGTATCCC AGGAGCATGG AAACGGGGCC 1440
TGGTGTGCAA CAGGTGCTCA GTAAACGGCT AAGGAAGGAA TGTCTGCCCA AGTCCCAGGC 1500
AGGGTGGGAG GCACGGACCT GAGGCAGCGC CTTCTCTTAG CTCTGAGCCC TGCCTTCGCC 1560
TCCTACAAGA TAGGATGGCA GCAGCCTCAG AGCAGAAGGC ACCCTGGTGA CCGCAGGAGA 1620
CGCCACACAT AAAGGCAGAG AACAGAGCCT GGTGCTAAAA ATGAGAGGGG ACAAGTGAAG 1680
CCTAAGCTGT TTCCGGGGCG CTCAGACCAG GCAGGGACTC AGGCGTGCAG CTGCCTGGGC 1740
ACCGCTTCAT TTCCCCCGGT GCCTCGGAGT CCCCGCGGGA CCTGCTGCTC AGCGGTCCAG 1800
CGTCACTCAG CCTCCCGCCT AGAGCGAACA GGACCTCCAG GTGCTCCCTG CAGGGGATTG 1860
AGCCATGGGT GGCCAGGACT CTAGCAGGAA CCCTCAGGGA GCCGGCTCTG CCTGGTGCAT 1920
GGGTCGAGGT GCTCATCAGT TTCAGAAGCT GCTCCCAGGC CCCCATTTTC CCAATCCCCT 1980
TAGAAGAGTT TTGTTCTGAG CTCCACTGAA GGTCATTTAG TCTTAAATGG AAGCAGGGAA 2040
CCCTCAGCTG TCACCCACGT GAAGGAAAAC CAGCTGAGGC CATGCCTTTG AGGTCCGGCG 2100
CTCCTCCCCC ACCCTGGGCC TCAGTCTCCC CATGGAGGTG CTGGCTATCC AGAGCCCTGC 2160
TGATGGCAGG CAGTCACCAG TGAGGCAGAC CCGGCCTGGA CGTTCTGGCT CAAAGGACAG 2220
GGTGCAGCCA GATGCCAACA CTTCCCTCCA GGGCAGGGGC CTGCAGCTGC AGAGCTTGGC 2280
TCTAAATAAC GCCAACCTCC TTGCTCTGCA CAGCCCTGGG GTGGCCCTGC AGTCCCCATG 2340
ACACAGGGCA GAGGTGCTGC CTTTGGGTGG GACGGCAGCC CTCCAGGAGA TGCACCCCTC 2400
ACAACCCACC CAATCCCTCT GCCCCTGCCC TGCAGAAGCC TGGTTAGAGC CCATAGCCTC 2460
ACTCTTCTGG GCCGCCGAGC ACTCCAGGGC CTCTATGCAA GTGAGGGGCA TGCGCTGGGG 2520
CCTCCCACAC CCTCCCTAGG TGCAATTCTC CTTGTCTCAT CAACTCGTCT CATCCTGGGA 2580
TGCGAAGGGT GGTCAGGGAC AGCCGTGTTC ATGAGCTGCC ATTTGGAACT GGCATTTGGA 2640