EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-34518 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr9:38025180-38027920 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr9:38026433-38026444GGATGACTCAT+6.62
JUNBMA0490.1chr9:38026433-38026444GGATGACTCAT+6.62
ZNF263MA0528.1chr9:38025512-38025533TTTTCTTCTCCTTTCTCCTTC-6.87
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00446chr9:38023728-38028204Adipose_Nuclei
SE_01843chr9:38023547-38028728Aorta
SE_02310chr9:38023662-38027951Astrocytes
SE_03893chr9:38021633-38029096Brain_Anterior_Caudate
SE_04803chr9:38021731-38029328Brain_Cingulate_Gyrus
SE_05785chr9:38021183-38028964Brain_Hippocampus_Middle
SE_06784chr9:38021571-38027567Brain_Hippocampus_Middle_150
SE_07767chr9:38021510-38029133Brain_Inferior_Temporal_Lobe
SE_23246chr9:38025987-38028588Colon_Crypt_1
SE_24298chr9:38025998-38028126Colon_Crypt_2
SE_26555chr9:38022184-38028472Esophagus
SE_27864chr9:38023794-38027403Fetal_Intestine
SE_28791chr9:38025361-38027128Fetal_Intestine_Large
SE_31580chr9:38025043-38027247Gastric
SE_33929chr9:38022707-38028095HCC1954
SE_34811chr9:38023130-38028698HeLa
SE_36884chr9:38023288-38028023HMEC
SE_38030chr9:38023941-38028420HUVEC
SE_38998chr9:38022657-38029283IMR90
SE_40993chr9:38025034-38027717Left_Ventricle
SE_41666chr9:38025120-38026517LNCaP
SE_41666chr9:38026590-38027990LNCaP
SE_42283chr9:38021564-38028766Lung
SE_44329chr9:38025101-38027892NHDF-Ad
SE_44779chr9:38023356-38028059NHLF
SE_45758chr9:38023295-38028397Osteoblasts
SE_47196chr9:38021414-38029507Panc1
SE_47459chr9:38025156-38025530Pancreas
SE_47459chr9:38025870-38027469Pancreas
SE_48861chr9:38023882-38027897Right_Atrium
SE_51847chr9:38025100-38027768Skeletal_Muscle_Myoblast
SE_55662chr9:38023553-38028534u87
SE_57367chr9:38025123-38028638VACO_503
SE_57926chr9:38026010-38026363VACO_9m
SE_57926chr9:38026673-38027099VACO_9m
SE_63571chr9:38025065-38027814HSMM
SE_64986chr9:38023280-38027960NHEK
SE_65279chr9:38024925-38028685Pancreatic_islets
SE_67542chr9:38023553-38028534u87
SE_69063chr9:38025056-38027553H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93802518038025621
chr93802563038027612
Number: 1             
IDChromosomeStartEnd
GH09I038021chr93802174938029286
Enhancer Sequence
CAACCACCCA TCGCTGTGGA CAGCTCTCTG TGGGAGGTGG GCTCCGGGCC AGGCTGGGTC 60
CCCATGGAGC CACTGACTTA GCCGCCCCTC ATTCTCCCCT CAACTCCTAC TTGGCTCTGC 120
TCAGCTCTCC TGCAGACTCC ATCAACCTCT GTCCACCTTG CCAGACAGCC CTTCCTCTCA 180
GGCTTCCTGC TCTAGGGGGT ACGAGTGCTC CCCTAGGGGC CTGAGGCGAC ACTTACCAGG 240
GACAGGGAAA ATGGGCCTGA GAAGGGTATC AGGAAAGCTG GTTACTAAGC CAGCTCTCAG 300
ACCAGCCCTG GTCGCGAAGA GTAAGAGCAA GATTTTCTTC TCCTTTCTCC TTCGGAGCTG 360
AAGGCTGGAA GGGTAAGGGG AAGGTACTAG TTAAGCTCAG GGTCACAGGT GCCGGATGGT 420
TCCACAAATC ATTTAGCCCT CTGCTCTCAC CCTCCTCATC TGTGAAATGA GGATGGGGCA 480
AGGCCTACCT GAGCCAACGC ACATGGTGTA TTCGGAACAG GGTGGTGCAC AGCAAGTGCT 540
CAGTGTCAGG TGTGATCACC ATCAGCTCAA CACACCATCC AGCCTGCAGA GTCTGGGTCT 600
TGCCCAGGGT CACCTGGACA TCAGAAATCC AGACTATCCC CCTCCCCATG TTGATGAGGA 660
GCCACCAGAG GCTCCAAGTA ACAAATGACA CAGCAGAACA CTCCTGAGCG GGTGACAGAA 720
CTAGACTCCC ATCAAATCCC AACCAGGAGA GGACCTATGT CATCTGTTGA ACTACATATT 780
TACAGAGTGC CTCCCAAACT GGTTTTAGAC AGCTTAATTC GAGGCATTTT TCTGCTTCTG 840
ATAGGCACAG CCTGTTGGTC CCCCACCCCC TTCCCAAGGA AGGATCAGGA ATGCCCGTGA 900
GGCTTTCTCA CGGTAACGTA AGGCTCTGTA CAGTAAGAAT AACTTCCAGT GTGCTCACAG 960
GAAAAGTATG TAAAAGCAAA ACAGCAGCGC CTGTGAGCCA AAGGCCTTTC CTGTGCAATG 1020
TGGTACCTTT CAAAGCCAGG CCTCTGTGCC CCAGCCAAGG CCCGGGAGTC ACCAAGTGCA 1080
CCCTCTCTCT CGTGTGTGCT TCCTGTGCTA GAAGCCAAGG TTAAAGGGGA GAAAGAGCTC 1140
AGGCCTGGAG GAGCACGAGA TCGGGCCAGC ACAGTGCCTT TTAATGATCA GCTGCAGAGG 1200
CGCGGGAACC CGCACTAAGT GAAGGATCAT TTCTCCCCGA ACGGGACCCA TTAGGATGAC 1260
TCATGCACAT TTCCCACAGG GGAGCTAAAA GGCTGGGCCA GGCCCCTTTA AGGCACAAGC 1320
AGCACTAAAC AGCTGCTCTC CCCAAGAGTC ACTCTCTCTT TATTGAGGAT AGGCAGCATC 1380
AGCCACAATT ACCAGCCCCA TGTTTGAGGG CTCCCAATTA CATTCCGCTT AACACCAGGT 1440
GCTCCATAAA TGCTGATTCA CTTTTTAAAA TAATGCTGTA TCCTCCAGCA ACCAAGCCTT 1500
GATGAACTCT TTCTCCTGTG CCGTCATCTA GGCTGGGAAA CCCTGAACCT CACAGGCCTG 1560
TTTCTCACAT GTACTCGGCG CTTTCTAATG TACAGGAAAC TTAGGGTGGC TAGGGCTTTG 1620
CGATGTCAAG CAGGTCTGTG ATGGTGTTTA TCGCTGTTCA GTCCGATCAC CTCGTGCCTC 1680
CACGTGCCAG GCAATGGGCT CTGTGCTGGG GATACAGAGG AGAGGAAAGG CAGGCCTCCT 1740
CCCCCTGCTC TTGCATTGCT TCCAGGTCCC CAGGGGAGAT GGGCATTATT CAGTTCACCT 1800
CCCCAAGGCA GGCTGGCATG TGCCAGGCAG GGTGAGTAAA TGCCTGGGTG AAGGGCCCTT 1860
CCCACCCTGC CCTGAATTGC AGCTATGTGT AGGCCTGTCT GCTTCCGCTC CACCAGGAAG 1920
GCAGGTTCTG GAGCTCTGTT TCCTTTTTAT TACAATATAG CACCTGGTGC ACAGCAGGGT 1980
CCCAGCAAGG TGTGCTGGGC TGAAACCAGG GGCAGGGCAG GGCAGGGCCT CCAGGGTGGT 2040
GGATTCCGGG CCCTGAGCTC CAATGCTTCC AAATTTCTCA CCAGCTATGG AGCTCTACTT 2100
TCTCTAAGCC TGAGCCCTCC CACTTTCACT GGGAAAACAT CTTCCTTCTG CGGTGCAGGA 2160
GAAGCTGAGT CAATGAACCA AGGGATACAT AGTGCCTGTC ACATTATGCT GGCATAGGCA 2220
AGGGCACAAG GGCACTAGAG AACACAGAAA AGATGCTGCT CTTATCCTCT AGAGGCCACA 2280
GGCCATGCCT TTTAGTCTGG GGAACCCAGA CACAGACCTT GAAGCAGGCA CTAAAATGCA 2340
AGTGGTTGAT CTGGGAGGAG ACACTTACCG GGGACAGGGA AAATGGGCCT GAGAAGGGTA 2400
TCAGGAAAGC TGGGTTACAA AGCCAGCTAC CCATGGTGGG CAACTAGATG GAGCATGATC 2460
TGACAGAGGA AACTCTGGGA AACCATGCAC AACCCACCCC TCAGAATTAC CTTACCAAGA 2520
GTGAGGGAGC TGGGGGTCAG GCACCAACTC CTGGGAGCTC CTGGTGTAGG CAGAGCGGCT 2580
GTTCCCATTC CTATGTTCTA GAAAAGCCCT CGGGCACAGA GATGTGGATG AGCCAGTTGG 2640
AGAAGGCCAG ACTGGGGAGG CAGAAGGGAC AGGGTGGGTC TTGACAGCAT CTGCTGCCCA 2700
GGGCAGGGGG TGCCTCCTGG AGAGGGATGG AGCTGAGCCA 2740