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

TagContent
EnhancerAtlas ID
HS187-00478 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr1:27881170-27883510 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr1:27883471-27883482GCCCCGCCCCC+6.02
KLF5MA0599.1chr1:27883471-27883481GCCCCGCCCC+6.02
Myod1MA0499.1chr1:27883126-27883139GGCAGCTGTCACT+6.04
ZNF263MA0528.1chr1:27882719-27882740CCCCTTCCCCAGCCCTCCTTC-6.12
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00527chr1:27880424-27884851Adipose_Nuclei
SE_00861chr1:27880860-27885523Adrenal_Gland
SE_01588chr1:27880381-27885646Aorta
SE_02913chr1:27881045-27881542Bladder
SE_03261chr1:27882696-27883339Brain_Angular_Gyrus
SE_03939chr1:27880687-27883623Brain_Anterior_Caudate
SE_05478chr1:27882535-27885308Brain_Cingulate_Gyrus
SE_05814chr1:27880294-27902223Brain_Hippocampus_Middle
SE_06945chr1:27881873-27884818Brain_Hippocampus_Middle_150
SE_07770chr1:27881026-27885690Brain_Inferior_Temporal_Lobe
SE_14757chr1:27880735-27883185CD4_Memory_Primary_7pool
SE_24168chr1:27882323-27882658Colon_Crypt_2
SE_24711chr1:27882295-27882975Colon_Crypt_3
SE_24711chr1:27883204-27885625Colon_Crypt_3
SE_25901chr1:27880642-27882323Duodenum_Smooth_Muscle
SE_26518chr1:27880547-27885700Esophagus
SE_27625chr1:27882781-27885755Fetal_Intestine
SE_28547chr1:27882782-27885683Fetal_Intestine_Large
SE_29557chr1:27880795-27885259Fetal_Muscle
SE_31394chr1:27880792-27885806Gastric
SE_33018chr1:27883160-27884329H1
SE_34367chr1:27883153-27885684HCT-116
SE_34755chr1:27882745-27885799HeLa
SE_36974chr1:27880413-27885442HSMMtube
SE_39896chr1:27880850-27881686K562
SE_39896chr1:27882052-27883493K562
SE_40593chr1:27879212-27885589Left_Ventricle
SE_42106chr1:27880393-27885776Lung
SE_46630chr1:27881333-27883136Ovary
SE_48058chr1:27880401-27885531Psoas_Muscle
SE_48567chr1:27880604-27885510Right_Atrium
SE_49444chr1:27881770-27882703Right_Ventricle
SE_50130chr1:27880522-27885676Sigmoid_Colon
SE_51091chr1:27880499-27885528Skeletal_Muscle
SE_52467chr1:27880855-27883297Small_Intestine
SE_54527chr1:27880582-27885136Stomach_Smooth_Muscle
SE_55184chr1:27881649-27882649Thymus
SE_55184chr1:27882706-27883969Thymus
SE_57312chr1:27883235-27885399VACO_400
SE_65253chr1:27880564-27884379Pancreatic_islets
SE_68682chr1:27881766-27883008H9
SE_68682chr1:27883179-27885755H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12788233727883453
Number: 1             
IDChromosomeStartEnd
GH01I027554chr12788064127885661
Enhancer Sequence
CTGACCTTGT TCACTGCCTA ATGTTTGGCT CTGACCTAGT ACTGGATCCC TGGGACCTAT 60
GTGCCACAGA CCCATGTAGA TTCTCCCCAC CTACCCATGC TGTCACCCCA CAGGAAGACT 120
GCAGAGCTGA CTCGGGGACA GGATAAAGTA GAAAGAGACA CTTCTCTACT CCCCTTTGGG 180
GGACAGCGAT TTGCAATCTA CAAAGCACCT ACACATCTGT GACCCACTGA ATCCTCACAG 240
CAGCCTGGGA GGCATGATTT ATTATCCCCA TGTTACAGGG GAAACTGGCT CAGAGTGTAT 300
GTGTAACTTG CCTGAAGTCA CATAGCTGCT AAGAGGCAGG ATTTCTAATT CTGCCTTAAG 360
TCCAAAGCCT CCTTCCACTC CCAGCTCCTG TAACAATCCT TCAGCCACTT CTGAAAATGC 420
TCCTTCTAGC GCCGTGGTCT AATTTAAGGC TGGGAGGAAC CTTAAAATTA TCTAACCCAT 480
TGGCTTCCAA AGCCTGGGCC TGGGGGAGCT GTGTAACATT CCAGATACCC AGGCCCTAGT 540
CCAGGGGAAT GTGACTCATA GATGTGAAGG GACATCTGGG AATCTGTATT TTTAACCAGC 600
TACCCCAGTG GGGACACTTT CTAGTGCCAT CTCATGCCCC TCCCATTTTA CAGATGAGGA 660
AACTGAGACT TGAAGAGGGA AAGAGACTTT GTCCGAGGTC ACAAAATGGC ACAGGAAGGG 720
GCCCTTTGGT TGCCCACCCA GGTGGAACAT CCCTCTATCC ACTGTTCCTT CTCTCTCTGC 780
AGGCTCCAGG ACTCAGCTGC TCCTCGTTGT CCCACCTACT GGTCCCACCT ACTTTGCTCT 840
CTCCCAGGCC TGGCTGTGGA CCTGGCCCCT CCCAGGTCAG GATCTCTCTA GTCCAAGAAC 900
TTGGAGCACT GTTGCCCTCA CAGGGAGGAC AGTGGGTGAC ACCCTCACAA ACGAGAAAAG 960
GGGCTCAGAC TCTGGAACCT CCAAGTCCAA TTTCCAACAG TGTGGTTGGG CCGTGGCTCC 1020
TGGCACCCAC TTGGAGATGC CCACCAGAAG CCCCCTCCCT CCCTCCCTTA CTGAGGGTCA 1080
GGCTAGCCGA GCCTTCCCCG CCCTGGAGAC CTCCCAGCTG GGGCCTGAGG GTGTGATCTT 1140
GGCAGAAGAG AAAAACCTCC TCTCCGGTGG TGGCTTCTGT TCAACCCACC CGTGAAGACC 1200
TCTGGGCACG TCCTCCTGCC AGGCCTCCTG AGGCTGGCCA CTGCTCTCTT TTGCAGCCTC 1260
CAGGATCTGA GGGAAACAGC TGGCTCCCCT CCTCACCACA CCCCGGCGGC CATTCTCTTG 1320
GACCCCTCCC AAGGGTACCA CCTAGCCCTG GTCTGTGGAC AAAGTCAAAG GGGTACTTCT 1380
GTCTGCCTGT CTGCTGTTGG GTCAGTGTGT CTGAGCTTGC CCATAGGGAC ACCAGCTGGT 1440
TGGGAGGGGG CTGGGGGCCC CAACCTGCTG TGCACAGTGC CGGGAAGCGC CAGCCCACAT 1500
CCTTGAGTCC CCAGCCCCAC CCTCCCCGGC TGTGGCTGTG ACCACCCCAC CCCTTCCCCA 1560
GCCCTCCTTC CCCTCCCCCA CCCACTGCCT CCCCAGGGGA GCCAGGCTGC CAGCCCCAGC 1620
TCTCACTTCC GGCCTCATGA CCCTCTCTCC AGCTTGCACA CTCCTCCTCC CCCACCATTT 1680
CCCTCCCAGC CTGGTTCGAA GGCCCTGGGA TGTCCTCAAA TGGAAAACAC TGCATCAAAG 1740
GGGCCATTAC TGCTGCTCTG AGACCTTCCC ATCACCTCCC TTTTCCTCCA GGGGCCTTAT 1800
CTCTCAGGAT CTGTCCCTCA GGGACTAGTC ATCACCTCTG TCCACCTCCT TCCCTTCAGC 1860
CGCCTACCTG CCCACACAGT AACACCTGAA TATCTTCTTT CAACCTGATC CCAGGCACAA 1920
TATCATAATA CAAATAACAA TGATGGCAAT AATAATGGCA GCTGTCACTC ATTTGGCATC 1980
ATTTAAATAG AGGCACAGAG AGGTTAAGTT ATGCCCTTAA GAACAAACAG CCATCTCATT 2040
CAATTAAGCT GGTGTCTGAA TTTAGGTTGG GCTTCTGTAA ATCAAACTTC TTTGGTGTCC 2100
AGAGATTCAG CGCCCTCCCC TGCAGCCTCC TACAACGGTC CTAGTCCCAA CCATCAGTTC 2160
TAATTTTTGA CTTCTAATCT ATCCTCCTCT CAGCTTCTAG TCACCACCTC CCACCAACAG 2220
CCATCCAACT AGATGCACTA CTCTCCCTCG CCACTAGGTG TCCCCTTGGA GCCACTGATG 2280
CCCCCAAGGG GAGCTGGCCC TGCCCCGCCC CCTGGGGCCA TCAGGGCCCC CCCACAGCAC 2340