EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS104-48570 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr5:131749940-131751430 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr5:131751231-131751243GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr5:131751235-131751247GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr5:131751239-131751251GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr5:131751243-131751255GTTTGTTTGTTT+6.32
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00037chr5:131744052-131766081Adipose_Nuclei
SE_09163chr5:131744997-131751563CD14
SE_10413chr5:131750032-131752061CD19_Primary
SE_10915chr5:131741116-131769232CD20
SE_11905chr5:131750328-131751351CD3
SE_13453chr5:131749973-131751107CD34_Primary_RO01536
SE_14574chr5:131750163-131751420CD4_Memory_Primary_7pool
SE_17470chr5:131750152-131754178CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131741156-131752202CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131741096-131752351CD4p_CD25-_Il17-_PMAstim_Th
SE_19972chr5:131742617-131754310CD56
SE_20885chr5:131743327-131751170CD8_Memory_7pool
SE_22284chr5:131740875-131754326CD8_primiary
SE_23079chr5:131750378-131751197Colon_Crypt_1
SE_25340chr5:131744602-131768034DND41
SE_25784chr5:131743830-131753894Duodenum_Smooth_Muscle
SE_26597chr5:131749787-131750249Esophagus
SE_26597chr5:131750359-131750952Esophagus
SE_27859chr5:131749789-131751505Fetal_Intestine
SE_28909chr5:131749730-131751413Fetal_Intestine_Large
SE_30917chr5:131750195-131751044Fetal_Thymus
SE_32566chr5:131745522-131752050GM12878
SE_37471chr5:131749954-131751679HSMMtube
SE_39368chr5:131750039-131751349Jurkat
SE_40726chr5:131750343-131751693Left_Ventricle
SE_42103chr5:131750281-131751628Lung
SE_43553chr5:131744726-131752486MM1S
SE_46095chr5:131745310-131751711Osteoblasts
SE_50034chr5:131750020-131751373RPMI-8402
SE_50051chr5:131750257-131751576Sigmoid_Colon
SE_52336chr5:131749794-131751276Small_Intestine
SE_53285chr5:131749764-131750231Spleen
SE_53285chr5:131750251-131751357Spleen
SE_59850chr5:131745223-131774088Ly4
SE_61542chr5:131744876-131774119Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_66244chr5:131750039-131751349Jurkat
SE_67252chr5:131744726-131752486MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131750200131751424
Enhancer Sequence
TCACCTGTCT CAGCCTCCCG AGTAGCTGGG ACTACAGGTC CCACCATGCC CAGCTAATTT 60
TTGTATTTTT AGCAGAGACG GGGTTTCACC ATGTTGGCCA GGATGGTCTC AATCTCTTGA 120
CCTAGTGATC CACCCGCCTC AGCCTCCCAA AGTGCTGGAA TTACATAAGT ATGTTTTCTC 180
ACGTCTCTTT TTCCTTACCT TTTCCCCACA GGCACATATA CACATAGGTA TCTGCCTGGG 240
AATTATTAAA ATAACCTGAA CAATTCCAAT TGTTATTAAT TCTTCTTGCT TCAAAATACA 300
ATTTCCTTTT TCTATGTTAG AAATATTAAC AATTGCATTA ATCTACAATC TAACCTATTT 360
GTGCAATTGC ATATTATACC AGGATAGGAA AGTTTAAACA TGTATTTCTT TTAGACTTTT 420
CATTGAATTG CTGAAAATTC ATAGTGAATT GTATCTTGAG TAATGCTTCT CTGAGTCTCT 480
TATTTCCCAA AAGTATACTT TGGAATCCAT GCAATTCTGA TCGTTGTTTG ACCTTTGCTG 540
GCACAAAGGC ATTCTGAAAT ATTTGCAAAT GCTAAAGTCA CTTCCTCATC TTTTACAGAG 600
TTTACTTCAG CTTGGTGAAA CCAAGTGCAG TATCAGTTTG TTGTAAGCTT ACCACTAATT 660
AAAGGTTCAT AAAATAGCCC TGCCCTAGGG TCAGGGACTA GCTAGAAGAG CATGAAAATA 720
GCCTTTGAAG ATTCAGCTGC TGGATATTTT ACATCAAAAA GCTGAAACGT TTTAACTATT 780
TTAATATTTT GTTTATAGTA CTTAATATTT GTGAACGTGA AGTAAAATGG ACACAGTCAT 840
AGTAAAACTG TGGTAAAACT AACTTGGATG GTGTTTGGGC TGTGGTTATC AGAAGCTGCT 900
TAAAGTGTCC ATGCCTTTTA TCCCAGTTCT ACTTCCAGGA ATATGTCCTA AGGCATGTTT 960
TCATATGAGG TTATTTCAGG TGGCGCAGGG TAATTCTAGT TGGGACACAT TTGCCACATT 1020
GTCTAACACT GACTCACAGT GAGAAAGTTA TTCCCATGCT CAATTCCTTT TCAGTCTTCT 1080
GATCAACGGA AGGTGAAAAA CTTTAGCTTG GTGCTAGCAT ACCTTTAACA CCTCTCTAAG 1140
CCTCTCTAAT CTCCCATTTT ATATAAAAGA ATGGGCAAAG GGGTAGCAGT ATTTTGACTA 1200
TATTTTAACC ACAGTGTTTT TTTATTCCAA TAAAACCTAT TATGATTGCC TTCATTTATG 1260
GCATATGATG TTGGTTTTCC ACTTAAATAA GGTTTGTTTG TTTGTTTGTT TGTTTTTTGA 1320
GACAGAGTCT TGTCCTGTTG TCCAGGCTAG AGTGCAGTGG CATGATCTTG GCTCACTGCA 1380
ACTTCTGCTT CATAGGTTCA AGCGATTCTT GTGCCTCAGC CTCTTGAGTA GCTGGGACTA 1440
CAGGCACGCA CCACCACACC CGGCTGATTT TTTGTATTTT TAGTACAGAC 1490