EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-58024 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr6:42738470-42739620 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr6:42739216-42739236CCTGTGGGGGTGGCGGGGGG-6
RREB1MA0073.1chr6:42739226-42739246TGGCGGGGGGTGGTGGGGGG-8.03
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_10484chr6:42738178-42740525CD19_Primary
SE_11266chr6:42735056-42740997CD20
SE_11972chr6:42738163-42740948CD3
SE_13047chr6:42739277-42740167CD34_Primary_RO01480
SE_13520chr6:42738238-42740256CD34_Primary_RO01536
SE_14202chr6:42738366-42739204CD34_Primary_RO01549
SE_14202chr6:42739228-42740111CD34_Primary_RO01549
SE_14568chr6:42736636-42741037CD4_Memory_Primary_7pool
SE_15495chr6:42738167-42740925CD4_Memory_Primary_8pool
SE_15889chr6:42737785-42739109CD4_Naive_Primary_7pool
SE_15889chr6:42739236-42740754CD4_Naive_Primary_7pool
SE_16414chr6:42737898-42741071CD4_Naive_Primary_8pool
SE_16944chr6:42738172-42740855CD4p_CD225int_CD127p_Tmem
SE_17402chr6:42736416-42740968CD4p_CD25-_CD45RAp_Naive
SE_17930chr6:42736416-42745788CD4p_CD25-_CD45ROp_Memory
SE_18745chr6:42736852-42740988CD4p_CD25-_Il17-_PMAstim_Th
SE_19398chr6:42738163-42740818CD4p_CD25-_Il17p_PMAstim_Th17
SE_20214chr6:42738162-42740932CD56
SE_20948chr6:42738197-42740786CD8_Memory_7pool
SE_21530chr6:42738234-42740848CD8_Naive_7pool
SE_22034chr6:42738170-42740953CD8_Naive_8pool
SE_22496chr6:42737298-42740811CD8_primiary
SE_24318chr6:42738594-42738979Colon_Crypt_2
SE_24948chr6:42738562-42739200Colon_Crypt_3
SE_27523chr6:42738366-42739166Esophagus
SE_32139chr6:42738372-42739233Gastric
SE_33171chr6:42738610-42739604H1
SE_42963chr6:42738372-42739244Lung
SE_43919chr6:42738112-42740596MM1S
SE_52994chr6:42738339-42740691Small_Intestine
SE_53635chr6:42738308-42739907Spleen
SE_55473chr6:42738393-42739227Thymus
SE_58803chr6:42738292-42759356Ly1
SE_59130chr6:42738290-42752751Ly3
SE_60114chr6:42737015-42755246Ly4
SE_60641chr6:42738286-42753091DHL6
SE_61049chr6:42738056-42753148HBL1
SE_62332chr6:42737059-42758313Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr64273853042739530
Number: 1             
IDChromosomeStartEnd
GH06I042769chr64273766842740635
Enhancer Sequence
CGGTCTGGAG TGCAGTGGCG CAATTTCCAC TCACTGTAGC CTCCACCTCC CGAGTTCAAG 60
TGATTCTCCT GCCTCAGCCT ACCGTGTAGC TGGGATTCCA GGTGCCCGCC ACCACGCCCC 120
GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAC GTTGGCCACG AACTCCTGAC 180
CTCAAGTGAT CCGCCTGCCT CGGCCTTACA AAGTGCTGGG ATTACAGGCG TGAGCCACCG 240
CACCCGGCCC TCCCCTCTCT GAACAGGATT GCCTACTCTG TCCTCCGACT CCCAGAGCTT 300
TTCACTGACA CCTGGGGACT GCTGGGTCCC TCCTTCTCTC CTAGCCTGCC CAGGGCCACC 360
CCAAGCCTGC AGTAGATTTT CATTTATCTC TGTAAGAACG TTTACAAGGA CATGGAGCAA 420
ATTAGCATCA CACAAATGAC GATGCTGCAA ATGAGCGGTG TACAGGGTTG GCGGGTGTTG 480
CAGGCAGGTT TCCTGTCGTT GGCGCCACGT GCTGCAGAAA GAGGACCCCT CCCCCTGCGG 540
GCCGCCGCTG CGCCCGTGCA TCCGTCACAG GTACAATTCG CACCGGAACT TGCGGCCCGG 600
CTTCATTACG TGATGCTTTT TAGCTGCTCT GGTTTCTTTT TGTTTTTTCT ACTTTTCTCA 660
TTTGTTTGTG TTGTTAGGGA CCGCCTAGTG AGAAATTGAG CTTCAGGCTG CGCAGATAGA 720
AAGGCCTCTA TATCTGCATC CCCACCCCTG TGGGGGTGGC GGGGGGTGGT GGGGGGGTCC 780
TGTCTGAAGT GGTAGGGAAG GAGGGTTTTG AGGTTTTTGA CTATTTGCTT GCAAGTATCT 840
AAGTAAGAGA TTTGTTTGCC CACATTTGCA CTCTCTTGGC TAGCAACCCG ACAAAATATT 900
TTCTGATGGT TTTTCGTGTA TGTGGTTTTT GTTTTTGAGG GAGAGAATAA TTAACACCTT 960
GGTTAAATTG TACTGAGATA CAATGGCTGT TTTTAAAAAT TGCTGTTAAC TGAAGGGTTG 1020
AAGCTAGTAT AATTCCCAGG CTCAGCCTCT TGGGAGGCTG AGTCTCCAAT AGCATAGTCT 1080
TCAATAGACT ATGCTGTGAA TTGTAATCAG AAAAGAAAAA AAAATTAGAC ACGAGCAAAA 1140
GCAATTAAAG 1150