EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS010-02187 
Organism
Homo sapiens 
Tissue/cell
B_cell_blood 
Coordinate
chr19:35695810-35696980 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:35696563-35696581CCCTCCTTCCCTCCTCTC-6.33
EWSR1-FLI1MA0149.1chr19:35696559-35696577CTTTCCCTCCTTCCCTCC-7.22
GATA2MA0036.3chr19:35696839-35696850TTCTTATCTCT+6.32
Gata1MA0035.3chr19:35696839-35696850TTCTTATCTCT+6.32
Gata4MA0482.1chr19:35696840-35696851TCTTATCTCTC+6.32
ONECUT1MA0679.1chr19:35696781-35696795AATATTGATTTTTC-6.76
ONECUT2MA0756.1chr19:35696781-35696795AATATTGATTTTTC-6.75
ONECUT3MA0757.1chr19:35696781-35696795AATATTGATTTTTC-6.92
SPI1MA0080.4chr19:35696386-35696400GAAAAGAGGAAGTG+6.92
ZNF263MA0528.1chr19:35696575-35696596CCTCTCCCCTCCTCCTTCTCT-6.54
ZNF263MA0528.1chr19:35696559-35696580CTTTCCCTCCTTCCCTCCTCT-6.88
ZNF263MA0528.1chr19:35696569-35696590TTCCCTCCTCTCCCCTCCTCC-7.65
ZNF263MA0528.1chr19:35696572-35696593CCTCCTCTCCCCTCCTCCTTC-8.15
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_10316chr19:35694706-35699540CD19_Primary
SE_11602chr19:35693742-35708404CD20
SE_11952chr19:35694362-35699527CD3
SE_14788chr19:35693951-35699612CD4_Memory_Primary_7pool
SE_15612chr19:35695871-35699271CD4_Memory_Primary_8pool
SE_15961chr19:35695886-35699340CD4_Naive_Primary_7pool
SE_16561chr19:35696013-35697479CD4_Naive_Primary_8pool
SE_20324chr19:35695762-35706055CD56
SE_21443chr19:35695519-35699393CD8_Memory_7pool
SE_21632chr19:35696466-35699556CD8_Naive_7pool
SE_22136chr19:35695876-35699598CD8_Naive_8pool
SE_22903chr19:35695804-35699515CD8_primiary
SE_43856chr19:35694166-35699480MM1S
SE_62877chr19:35694122-35708296Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193569637335696472
Number: 1             
IDChromosomeStartEnd
GH19I035202chr193569341435699474
Enhancer Sequence
ACCATAGAGG GTAACTTCCC GACATCGCCA TGGTATTTGT AAACTGTCAT GGCGCTGGTG 60
GGAGTGTAGC AGTGAGGACG ACCAGAGGTC ACTCTCGTGG CCATCTTGGT TTTGATGGGT 120
ATTATCTGGC TTCTTTATTG CATCCTGTTT TATCAGCAAG GTCTTTATGA CCTGCATCTT 180
GTGTTGACCT CCTATCTCAC CCTGTGACTC AGAATGCCTT AACCATCTGG GGATGCAGCC 240
CAGTAAGTCT CAGCCTCATT TTACCTGGCC CCTACTCAAG ATGGGGTTGC TCTGGTTCAA 300
ACGCCTCTGA CAGGGTGACA ACTGTGACCA CAACAGATTC ACAAACATGA CATTTTCAGA 360
GAGAGGAAGG TATGCAGGGT GGTGTGATTT GGAAGAGGCT GTGGGCGTAG AGGGATGGGT 420
AATTCAGTTG GGGTGGTCAG GGAGGGCTGC TTGGTGGAGG GGACTCTTGG CTGAGACCTG 480
AGGGCTGTGA AGTTCTTAGA GAAGGGTGTT CCAGGCAGAG GGAACAGCAA GCACAAAGGC 540
CTGAGACGAG AGCTAGCTTG GTATGCAAGA GGAACAGAAA AGAGGAAGTG AGAGTAAGGC 600
GGGGGAGGGA AGGGGCAGGG AATGGAGGCT GTGGAGAGGG GAGGGTTTCC AGGCAGCCCA 660
GGACCCTCAA GGAGAGAAAC GTTGGATGTA GTCTCCCAGG TAGGGTCCAT CTGGCCCTTC 720
CTCCTGGCTC CTGCGGAGTC CGAGTGGCTC TTTCCCTCCT TCCCTCCTCT CCCCTCCTCC 780
TTCTCTCCCT CTCCATTTTC CCTGCAAGGT CTGCAGCCCA ACTCCAGCTC TCCCATTACT 840
ACAGGGGCTG GTGGGTCCTT CTGAGCAAGA AGATGGGGCT CTTTGTCTAC AGTGTCTGTC 900
TATAGTCATT CACCCACTCA TTCATTTAAT CATTCACTCA TTCATTCATT CATTTAGCCA 960
CTCATTTGTC AAATATTGAT TTTTCTCAGG TGTTTTGCCC TCACAGGTCC TGCCGCCTAA 1020
AACACTGACT TCTTATCTCT CAAGGCTTTG CTTTCAACAC TGTCTCTTCC AAGACCTCTC 1080
CCTGACCACT CCCAACTTAC TAAACCCCTA TCACCCTGTT AGCTTTTGAA TGCTCTTCAT 1140
GGTAAAACAG GACAGGTTGA TGCTCTCCGG 1170