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

TagContent
EnhancerAtlas ID
HS018-24053 
Organism
Homo sapiens 
Tissue/cell
CD19+ 
Coordinate
chr9:123682330-123684560 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2269060chr9123683569hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr9:123684458-123684469TGTAAACAAGA-6.02
RELAMA0107.1chr9:123684071-123684081GGAAATTCCC-6.02
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_01292chr9:123680926-123682966Adrenal_Gland
SE_01292chr9:123683015-123683684Adrenal_Gland
SE_01292chr9:123683981-123684525Adrenal_Gland
SE_01664chr9:123680685-123684564Aorta
SE_04446chr9:123680706-123683695Brain_Anterior_Caudate
SE_05342chr9:123674762-123684591Brain_Cingulate_Gyrus
SE_06145chr9:123680720-123684735Brain_Hippocampus_Middle
SE_08512chr9:123680670-123683496Brain_Inferior_Temporal_Lobe
SE_11823chr9:123681415-123697392CD3
SE_15020chr9:123680779-123692584CD4_Memory_Primary_7pool
SE_15500chr9:123681522-123692469CD4_Memory_Primary_8pool
SE_16326chr9:123681322-123692243CD4_Naive_Primary_8pool
SE_16854chr9:123681565-123685232CD4p_CD225int_CD127p_Tmem
SE_17311chr9:123680688-123701002CD4p_CD25-_CD45RAp_Naive
SE_17766chr9:123674711-123700821CD4p_CD25-_CD45ROp_Memory
SE_18313chr9:123675977-123700962CD4p_CD25-_Il17-_PMAstim_Th
SE_19108chr9:123680709-123699940CD4p_CD25-_Il17p_PMAstim_Th17
SE_20050chr9:123681213-123683628CD56
SE_20050chr9:123683797-123696495CD56
SE_20905chr9:123681287-123692470CD8_Memory_7pool
SE_21626chr9:123681499-123684867CD8_Naive_7pool
SE_21944chr9:123681434-123685136CD8_Naive_8pool
SE_22312chr9:123679588-123700473CD8_primiary
SE_26506chr9:123680621-123683843Duodenum_Smooth_Muscle
SE_26718chr9:123680765-123683699Esophagus
SE_26718chr9:123683748-123686514Esophagus
SE_32579chr9:123681342-123699293GM12878
SE_43058chr9:123680751-123683548Lung
SE_43058chr9:123683701-123684556Lung
SE_49159chr9:123680700-123684577Right_Atrium
SE_50248chr9:123680844-123683654Sigmoid_Colon
SE_50248chr9:123683668-123684658Sigmoid_Colon
SE_52520chr9:123680686-123684572Small_Intestine
SE_53449chr9:123680700-123683512Spleen
SE_58895chr9:123680733-123708417Ly3
SE_61111chr9:123630545-123707493HBL1
SE_62230chr9:123630172-123700621Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr9123683790123684415
chr9123684222123684378
chr9123682864123683506
Number: 2             
IDChromosomeStartEnd
GH09I120921chr9123683879123684278
GH09I120918chr9123680990123683506
Enhancer Sequence
ACAGATGAAC ACTGTCAAGC TCAGAAGTGT AAGGTTTGGG GGTTTATTCC CAGGTATCAC 60
ACTTCAAGGA ACACAGATAA ACAGAAGCGC ATTTACCCCA AATGCACAGA GACTGGGGAA 120
AGACTGCTCA GTGTCTTTCC ATGGAGGCAG GACTGACTCC AGGGATAGGA GGCTAAGTTG 180
CCTTTTGTGA CCTCAAGGGA GACAGACAGA CTTCAGCTCA GTACAAAGAA AGAGGAGAAT 240
GTTGCATCAC TCAGAGCTCC CCAGGGTAGG TGTGGTTGTT TCATGGAGTA ATGACCTCTC 300
TGCCATTGGA AGGACATGGA GCCACGTAGC ATGAATCCAG TACAGAACAG AAATTGGACT 360
AGACAGCTTA AACCCTTGTC ACTTTCTGAG TCTAGACAAA TTAAGGCTTT ACTGTGAGCT 420
ACTGGCATCA GTTGTCAGCT TGCTTTTGAC CTTCTTGAAT GGGCCTCAGG GGGAGGGGGT 480
GGGAGAAACA ATCCCATTTG CTGATCCTCA GCAGACAGGA CTGAAGATTA TCTCCAGCCC 540
CCTGGCATCC CCTCCTTCAC TGTCACTTCT ACAGGAAGAT CACGCCAGGC AAGTATCAAG 600
TCTCTAACTA GGTCAACATT AATCCTCTAA TATCTGCTTC TTACATTAGG TAATCAGTCC 660
ATGGCTCTGG GCACTTCTTT GGGAGATAAT CATCTAATGA AGTCACAGGC TGGGGACAAA 720
CTGATAAGCA GATGGCATGG GAAGTGTTTG CAAGGAGGGC TGGTCCTCAG CCCTCCACCC 780
TGCCTCCATT TCCCAGGTTG CCCCAGATGT GCAGGCAAAC TTAGGAATTA CCACACATGC 840
AAAGTGGTGA CTTATCATCA GCCACTTTCC TTTGGTCAAA AGTCCCCCAA AGTTCCCACT 900
GGGGCAAAAG TCAGAGGAGT CCCTGGTCCT TCCCCTATGT GGCTTTGTGT AGGTGATCAG 960
ACCATGACTT ACCGCCCCTC CCCACCCCAG CTTTTCACCA GAAGTCCATG ACTCCACGAG 1020
GTGGGGAAGC CAGCAGGGAG GGGAGGGGGC TGATGCCTCT CAGAGGTCTG CCCGCATTAA 1080
AGAAGGCTTC TTTGCTCCCA AATACAGGCA GCTTCCTCTC CCATCCTGTA GCCTGTTAGG 1140
GTGCCTATAA TTCTACCATG AATTATAGTG CCTTCACTTG GCTTAAGGCA GCAAGTTTCA 1200
AACTGTGCTC TGCAGGGCCC TAGGAGTCCC CAGAACCTCT TAGGGGCTCG GATAGGAGAA 1260
AGAAATGGGG CAATTAACAG GTCGGGGCTC CAGGATCCCC CTCCATCAGA ATGCTTTTAC 1320
TTTCATCTGA TTGAAAAAGA TGAAAAAAAG CCATTGGATT AGGAGATATT AAAATATCTA 1380
TGTGATCTAA GATTTACACA ATAAATGTGT ATTAATTTTG TTAAGAGGAA AGAATAAAAC 1440
AAGCTAAAAA CAACAGTCCT AGAGCATTCA AGCAGGTAAG GGCCTTTTGC AAGTGAGGCA 1500
TAGTGGCTCA CAGAGTTGAG GGTCTGCTTG TGTCTCACAG CCGATCCACC AAGAGCCAAA 1560
CAGTGAGGCT CAGGGAGTTA CTCCACGGAG CAGCATATCA TATTAACTCT TACCACGTTG 1620
CAGAGTGTAA AGTTCCAAGA ACATGCATTT GGTCCTTACT CTTACTCTCT GAGGGCCTGC 1680
CGATGGAGAG GTTGCTGAGA AGCAGATGGG AGAGTGCTCA AAACCAGCTC TGGGTGGGAC 1740
AGGAAATTCC CCTGAACTCT CTGAATGAGA GGGACCAGCT CAGAGAAAGG AGAAGGAGGT 1800
GTGGACACTC GCCTGCCTCT GGTCCAGCGG TAGGGGGATA GCTGCCCTGC CAGCACTGCT 1860
ATCACGGTCT GGACATCACA GATCCTGGAA AGGCCTTGCA GAGCTGACTT AATATCCTCA 1920
TTTTACAGAT ACAGAAACAG GGCCTGGGAA TTGCTGCTAG CCAAGCAGAG AATTATGCAG 1980
AACCACCCCT GGACATCAGG CTCCTGATCC CTGGGCCACA GTTTGCTGCA AGAAGAGGGC 2040
TTTGGCTGAA AGGAGCCAGG CACTTCCCAG TGGAGGTAGA GAGGGCGGCT GAGCAACGAG 2100
ACTCCTCTGC AGGTCTCAGG GCCCCGTGTG TAAACAAGAG GATTTGATTT TGAGCAGTGA 2160
CTCCTGCCTG TTTGGATTCG TGGACCAATA CGAGTGTGTT TTTTTTTAAA TTGAGAGATT 2220
AACAAAGAGA 2230