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

TagContent
EnhancerAtlas ID
HS098-36726 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr22:30707310-30708870 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SOX10MA0442.2chr22:30708539-30708550AAAACAAAGAA+6.62
SOX10MA0442.2chr22:30708582-30708593AAAACAAAGAA+6.62
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00207chr22:30696033-30714616Adipose_Nuclei
SE_01017chr22:30706695-30709458Adrenal_Gland
SE_01933chr22:30704755-30709496Aorta
SE_03076chr22:30705469-30707709Bladder
SE_03076chr22:30707877-30708390Bladder
SE_06187chr22:30705172-30707851Brain_Hippocampus_Middle
SE_11435chr22:30693586-30712890CD20
SE_12307chr22:30699489-30707598CD3
SE_12307chr22:30708349-30709320CD3
SE_15119chr22:30704052-30707762CD4_Memory_Primary_7pool
SE_15119chr22:30707987-30709532CD4_Memory_Primary_7pool
SE_16208chr22:30708123-30709338CD4_Naive_Primary_7pool
SE_18199chr22:30696796-30709288CD4p_CD25-_CD45ROp_Memory
SE_19840chr22:30703973-30709406CD4p_CD25-_Il17p_PMAstim_Th17
SE_22773chr22:30696696-30709496CD8_primiary
SE_23721chr22:30705436-30708802Colon_Crypt_1
SE_25730chr22:30696761-30709491DND41
SE_26571chr22:30696437-30709562Esophagus
SE_31521chr22:30703991-30709477Gastric
SE_34216chr22:30705635-30709402HCC1954
SE_39484chr22:30705418-30707852Jurkat
SE_39484chr22:30708593-30709395Jurkat
SE_41271chr22:30705407-30708762Left_Ventricle
SE_41665chr22:30705417-30707947LNCaP
SE_41665chr22:30707972-30708489LNCaP
SE_42270chr22:30703944-30709448Lung
SE_47044chr22:30705465-30707545Ovary
SE_47736chr22:30705437-30707875Pancreas
SE_48841chr22:30705238-30708514Right_Atrium
SE_48841chr22:30708530-30709327Right_Atrium
SE_50213chr22:30703979-30709498Sigmoid_Colon
SE_53095chr22:30703979-30707919Small_Intestine
SE_53095chr22:30708434-30709284Small_Intestine
SE_55187chr22:30707128-30707691Thymus
SE_55187chr22:30708448-30709442Thymus
SE_63164chr22:30696999-30708171Tonsil
SE_66498chr22:30705418-30707852Jurkat
SE_66498chr22:30708593-30709395Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223070792930708500
chr223070816830708313
Number: 1             
IDChromosomeStartEnd
GH22I030300chr223069653430717414
Enhancer Sequence
CCTGACGCCA CACACTCTGT GAGTTGGTAG GAAAAAGGAA GAGGGTCTGC AGCAGCCTGG 60
CACTCCCTTC TGGGGCCCGG CCACCCCTGC CTAGGAGCCG GCTGGCAGTG TCCAGGCTCC 120
CTGTCTGAGT GAGAGAGTCT GGCTTGCTTC ACTCTCCCTC CTTCCCAATG CAGGCTAATT 180
CTGGGGCTGC CTGTCTTTCC CATGAGGAAT TCCCTGGCTC TGCTCCTTCT AGTGCTGGGT 240
CAGTGCACAA TGGTAAACAG GTTCTCTCCA CCCTTCACTG GCCTTGGTGC CCTGGACCTC 300
TGCCCAGCTC TCTACTCTGC TCAGCTCCAC CCTACTCAGT GTGAGAAATG GTTCCTTTAG 360
CACTAGCCTT GCTGGCTCCC AAAAAGAAAA ACCAAGGTAT CTACCTTCCT CTGATGCACT 420
CATCTAGGGA AGGGCGTAGA CCACAGAGAA ACTCCCAAGC AGCTCTCCCT GACAACTGCA 480
GAAAGGTATT AGATAGGGTC TTGCTCTGTC GCCCAAGATG GAGTGCAGTG GCATGATCTC 540
GGCTCACTGC AGCCTCCGCC TCCTGGGCTT AAGCCATCCT CCCACCTCAG CCTCTCGAGT 600
AGCTGGGACC ATAGGCTCAT GCTACCATGC CCCACTAAGT TTTGCATTTT TTGTAGAGAC 660
AAGGTTTCAC CGTGTTGCCC AGGCTAGTCT CAAACTCCTG GGCTCAAGTG ATCTGCCTGC 720
ATCAGCCTCC CAAAGTGTTA GGATTACGGG TATTAGTGAC TGAGTGCCGC CTGAGACTAT 780
TCTCAACAGA AGACATCTTT TCTCCAAATC CCAGCTCCTA CCAGGCAGAG TGCTGCTTGA 840
AATTCCCTTG CTGGTGACTG AGTCCTTGGA TCACAATCTC ACTGCAGGCA CCCAGGGGCC 900
ACCCTGACTC ATCCTTACCA AACTGCTAGA TCTCATTGAT AGATCTTACC AAAATTAGTC 960
TTGACTCACT GTTTATATAA GGCCCCTCCT CTGCCCAGAC TCGTCCATGG CTCCCTACTG 1020
CCCTCATTAT CCAACAGAAA CCTCAGACCC TGTAGCTGGG CATTACGGCA CACGCCCTGT 1080
CATCCCAGCT GCTCGGGAGA CTGAAGTGGG AGGATCACTT GAGCTCAGGA GTTTGAAGCT 1140
GCAGTGAACC ATGATTGTGC CACTGCACCC TAGACTGGGC CACTGGGTCA CAGGGCAAGA 1200
CCTTTTCTCA AAACAAACAA AACAAACAGA AAACAAAGAA CAATAACAAC AACAACAACA 1260
AAAACAACAC AAAAAACAAA GAAACTTCAG GCCCTGGCTC TCAAGGCCCT CCTGTTCCCC 1320
TGCACATCCC TTTCTCCCCT AGTCCCATCT CTATAGGCCC CTACCCCTGA GCCATCTTCC 1380
TTCAACCCCC ATTCAATTTT GGTGCCATCA TCTTGGGAAG CATCATTCCA AACTCCTTCT 1440
CATCTCTACA AAGCCTCTCC TAACTACTCC AGGGACAGAA CACAATCAGG CCCTCATTAT 1500
ATTCCATGCA CACCTTTCTA GAGCCTGTGT TCCAGGCCCT GAATCTACAA AGATGAATAA 1560