EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-15468 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr17:75389880-75391350 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr17:75391109-75391120CCACACCCTCC+6.32
Nr5a2MA0505.1chr17:75390685-75390700TCTGACCTTGGGCTC-6.05
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00752chr17:75390032-75391185Adipose_Nuclei
SE_00855chr17:75389925-75391405Adrenal_Gland
SE_02266chr17:75389885-75391379Astrocytes
SE_02895chr17:75390240-75391066Bladder
SE_05840chr17:75389719-75391512Brain_Hippocampus_Middle
SE_18261chr17:75390046-75390824CD4p_CD25-_Il17-_PMAstim_Th
SE_23764chr17:75389922-75391279Colon_Crypt_2
SE_25342chr17:75390030-75391002DND41
SE_26523chr17:75389864-75391390Esophagus
SE_28815chr17:75389837-75391362Fetal_Intestine_Large
SE_29570chr17:75390093-75391469Fetal_Muscle
SE_31375chr17:75386752-75391593Gastric
SE_35553chr17:75386670-75392192HepG2
SE_36906chr17:75389814-75391492HMEC
SE_36938chr17:75383859-75394273HSMMtube
SE_40707chr17:75389823-75391432Left_Ventricle
SE_42146chr17:75389827-75391424Lung
SE_44144chr17:75389834-75391433NHDF-Ad
SE_44761chr17:75389819-75391295NHLF
SE_45597chr17:75386688-75391399Osteoblasts
SE_46677chr17:75389921-75390994Ovary
SE_47187chr17:75389845-75391652Panc1
SE_47590chr17:75389903-75391375Pancreas
SE_48637chr17:75389907-75391347Right_Atrium
SE_50053chr17:75389846-75391354Sigmoid_Colon
SE_51876chr17:75389956-75391131Skeletal_Muscle_Myoblast
SE_52347chr17:75389854-75391359Small_Intestine
SE_53286chr17:75389834-75391493Spleen
SE_54499chr17:75390080-75391300Stomach_Smooth_Muscle
SE_62213chr17:75358289-75491858Tonsil
SE_63645chr17:75389942-75391220HSMM
SE_65344chr17:75387658-75391416Pancreatic_islets
SE_68672chr17:75389967-75391327H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177539024875391136
Number: 1             
IDChromosomeStartEnd
GH17I077379chr177537510975393825
Enhancer Sequence
TGGTCTCGAA CTCCTGACCT CAGGTGATCC ACCCACCTCA GCCTCCCAAA GTGTTAGGAT 60
TACAGGCATG AGCCACCGCG CCTGGCCTCA GGGGCACCTT ATTACCCCAT CACCTCCTAC 120
AGCAGGTGAC ACTGAGGACA CTGAGGCTCA GAGTAGACTG TGGTTATGTC ACTCTCCTGT 180
TTGGTTCTCC TGCTCTCAGC CCTGAAATAA AGAGCACGGT CCCTGTGCAG GCCCATACGT 240
CCTGTCTCCA GCCCTGGAGC AGTCCTTAAG CTCCTTGAAG GCACACCAGG CCTTTGGGCC 300
TCGTCCCCCA AGTCCTGGAT AAATAGGAGG TGAAGGAGCC TTTGCAACTG GACCCCACTC 360
TGCCAGCGCC AAGGCCCTGC CTGACTACCC ACCCCACCCT ACACAGATCA GGGACCTGTG 420
CCAAGGTCCA GTGTCACAGG AGAGTGAAGA CAAGGAGGTG CCCATGGCGT ACATGCTGCT 480
GGACTCACTC TGTAGATCCT AAGGGTTATG GGGAGTTATC TGCCAGGTGA GGTTTTCCCG 540
TGGCTTTTTC CTGCAGGCTC AGGGTAGCAT ACAGGGAGGT GCTTCCCTAC TCCTTGGCAC 600
CATCTGTCCG GCTTCCCTGA GCCCTGACCC TGGCTCCTAG ATAGCCAGTG TTTCTTCAGG 660
GACAGAACCT GCTTTGCTGC TGCTCAGAGG AGACCCAGTT TGACCAGGGC TAGCGTTCCT 720
GGAACCTGAG CCTGGAATTC CACCCTGCCC TGGGCAGAGG CCACGTTGCT CCCTCCTACG 780
AGAGCTGAGC TGCGCATGAG ATTATTCTGA CCTTGGGCTC TACCATTTCT TTGCATGACA 840
TTTGTCCCAG GCTGGAGCAG GGCTCTGTGG CTCGCTTGGT GTTCCCTCCC CAGACTGAGG 900
CCTGATATGT ACACCAGGAA GTGCTTGATC TGGTTTCAGG AGCTGGGAGC GGTTTGCCAG 960
GCAGCCTGTG GTCAGAGCAG GGGCCTTAAC AATGGTCCCT TGTGCGGCAC ATTCCTCTCT 1020
AAATAGGCCC AGGTCCAGGC TGCTCCTGTT TCGACCCCGC CATGGGCCTG GAGGGGAAAG 1080
TTTGCATCTG GAGGGTGGCC CACTGTGGCC TCTTTTTGTG TAGCAGCTGA GACCGTAGGT 1140
GCTTGAGAAT AGGAGAAGCC CTGTGCCCAT CCTGGGCTGT GAGATGTTTT TCCAGAGGTG 1200
GGGATGGGGA TGGGCCAGCA TGCAGTTACC CACACCCTCC AGCTTGTTGG CATCAAGGTC 1260
TGTGTATGTG TGTGTTTTTT TTTTTTTAAT TTTGTTTTTC CAACATGGAG TCTTGCCATT 1320
TGCCCAGGCT GGTCTCGGAC TCCTGGCTCA AGCGATCCTC TAGCCTCAGG TTCCCAAAGT 1380
GCTGGGATTA TAGGTGTGAG CCACCATGCC CAGCCAGTAC CAAGGTGTGT TTTTTAAGAG 1440
CAATATTGGC CGGGTGCAGT GGCTCACGCC 1470