EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS103-10056 
Organism
Homo sapiens 
Tissue/cell
HUES64 
Coordinate
chr17:38490430-38491900 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr17:38491669-38491680GGTGACTCATG+6.62
HEY2MA0649.1chr17:38491807-38491817GGCACGTGTC-6.02
JUNDMA0491.1chr17:38491669-38491680GGTGACTCATG+6.02
Npas2MA0626.1chr17:38491807-38491817GGCACGTGTC+6.02
RREB1MA0073.1chr17:38491298-38491318GGGCTGTGTGTGTTTTGGGG-7.31
ZNF263MA0528.1chr17:38491022-38491043CCCTCCTCCCCCTCATCCCTT-7.08
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00190chr17:38489901-38492131Adipose_Nuclei
SE_00975chr17:38490962-38491667Adrenal_Gland
SE_01678chr17:38489878-38491777Aorta
SE_02972chr17:38490488-38491700Bladder
SE_04480chr17:38490803-38491417Brain_Anterior_Caudate
SE_06212chr17:38489778-38491899Brain_Hippocampus_Middle
SE_08413chr17:38490023-38491418Brain_Inferior_Temporal_Lobe
SE_09193chr17:38489586-38492655CD14
SE_10906chr17:38490026-38491898CD20
SE_14465chr17:38489838-38491680CD4_Memory_Primary_7pool
SE_17354chr17:38489961-38491142CD4p_CD25-_CD45RAp_Naive
SE_17774chr17:38489834-38491631CD4p_CD25-_CD45ROp_Memory
SE_19121chr17:38490020-38491719CD4p_CD25-_Il17p_PMAstim_Th17
SE_25879chr17:38490656-38491906Duodenum_Smooth_Muscle
SE_26766chr17:38490396-38491710Esophagus
SE_29564chr17:38490697-38491803Fetal_Muscle
SE_31511chr17:38486156-38492308Gastric
SE_33936chr17:38490128-38491787HCC1954
SE_34507chr17:38490461-38491821HCT-116
SE_35094chr17:38490589-38491992HeLa
SE_38107chr17:38490895-38491989HUVEC
SE_41732chr17:38490104-38491199LNCaP
SE_42126chr17:38489907-38491772Lung
SE_44282chr17:38490759-38491799NHDF-Ad
SE_44952chr17:38491016-38491745NHLF
SE_45871chr17:38490561-38492337Osteoblasts
SE_46732chr17:38490111-38491620Ovary
SE_48093chr17:38489780-38491792Psoas_Muscle
SE_48589chr17:38489937-38491745Right_Atrium
SE_50100chr17:38489978-38491780Sigmoid_Colon
SE_51122chr17:38485628-38492123Skeletal_Muscle
SE_52419chr17:38490110-38491766Small_Intestine
SE_53319chr17:38485880-38492398Spleen
SE_54720chr17:38489976-38491814Stomach_Smooth_Muscle
SE_59903chr17:38465110-38509835Ly4
SE_61531chr17:38458893-38531888Toledo
SE_62713chr17:38462659-38504649Tonsil
SE_65331chr17:38490005-38491764Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr173849060038491784
Number: 1             
IDChromosomeStartEnd
GH17I040333chr173848985338492252
Enhancer Sequence
AGAGGTGGGT GGGGAAGGCT TCCCATCCTG GTAACCTTCT CCCCAAATGT GGGTGGGGTG 60
CCCACATTTC AGGCAAGTGT AGCCTTCTTC GGCTTTCTCC ACCCAGGTTA GGCAATGCCC 120
CCTTCCTGCC CCCTCCCTCT GTGAGCCTTT TGGTTTCCCT GCCCCTCCCC TCTCCCTAGT 180
AAACAACAAC AACTTCTCTC CCTGCCCAGA CCCTTAGCTT CTGAGCTTCT CACTGACCTT 240
CCTCTTCTCT GGGACAAGGT GTGGCCATGG GTCTGAGGGA GCCTGGCATC TCCCTCCTTC 300
TGCAGAGCCA GGGCTGCCTG GTGGACAGAG CTCCTGAGCT CTGAGTAGGA AAGCATGGCA 360
GATAAAATTA TCACATGCCT GGCCTCAGAG ATGGAGGCAG TTTAGCCTTC CCTGCTTGCC 420
TGGCCTTAGG GCTGGTGCTG AGGGTGAGGC AGTTCCCAGG AGAGGTGGCA ATCCATGGTC 480
CTCCATTCCT GCAGGAGCAG TGGTATGCCC CAGTCTGCCC ATACCCTTTT TGTAGGAATT 540
CTTGCTGATG AGGCTTCCTA CTCCCATTCC CCATCCAACA AAGGTGTTGG GTCCCTCCTC 600
CCCCTCATCC CTTTCCCCAG GTGGGGAGGA GGCAGCACAT TAGGTGGCCT GGGTGCGCCC 660
TTCAGAGACC TAGTAGCCTA TGGGACCAAC AGAAACCCTC TCCAGGTCAC TGTGGGGAGG 720
GCTGTGTATT TGTTCTGCTA CAGCCAGGGT GGGAGCCCTA GAGATGGTCC GGCGATTCTC 780
CCCGCCCCCT AAACTGGCCC CTGGGGCTTG GTCTCTGAAG ACTGGTGTTT ACTGTGGAGG 840
TCTCAGATTC TGTGTGCACT ACGGGTCAGG GCTGTGTGTG TTTTGGGGGT GGGGTCACGG 900
TTGGGTGTGT GTTGGGAAGG GGATTAATGA CTTGTGTGTA TTGGGTGAGA GGGTTAGAGA 960
GCTGAGTGTG TTTTGGGGGA ATTAAATCCA GAGCTAAGGA GGGAGAGTCA GCCTGTCTGT 1020
GTGTTGGTGT TGGGGCTGGG AGGGGGAGTG ACTTAGGGCA CAGAGTGTTT AAAGAGGAGT 1080
GGTCTTTCGT TTGGGTTCTT AACCTTTCTT GGCTGGAGGG GAGAACTGAT CTGCCTTTTT 1140
TTGTTCACCC TGGGAATTCC ATGGGCAAAG GGGTCTGACT GGGGGCTGTG GAGTAGGCAT 1200
TTAGTGCTGA GTTTAAAACT TGGACACTGG GCTGGGCGTG GTGACTCATG CCTGTAATCC 1260
CAGCACTTTG GCAGGCCAAG GCGGGCGGAT GACCTGAGGT CAGGAGTTTG AGACCAGCCT 1320
GGCCAACATG GTGAAACCCC ATCTCTACTA AAAATACAAA AATTAGGCAG GCGAGGTGGC 1380
ACGTGTCTGT AATCCCAGCT ACTCGGGAGG CTGAGGCTAG AGAATCGCTT GAACCCAGGA 1440
GGCAGAGGTT GCAGTAAACC GAGATCATGC 1470