EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS018-03447 
Organism
Homo sapiens 
Tissue/cell
CD19+ 
Coordinate
chr10:126381960-126384240 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs11245333chr10126383088hg19
rs4450131chr10126383363hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr10:126382824-126382835TGTAAACAGGA-6.62
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00867chr10:126382460-126383468Adrenal_Gland
SE_03059chr10:126382298-126383494Bladder
SE_03136chr10:126382036-126384047Brain_Angular_Gyrus
SE_03854chr10:126381278-126400264Brain_Anterior_Caudate
SE_04762chr10:126349641-126400539Brain_Cingulate_Gyrus
SE_05766chr10:126349634-126432936Brain_Hippocampus_Middle
SE_06675chr10:126352052-126400411Brain_Hippocampus_Middle_150
SE_10231chr10:126381919-126383539CD19_Primary
SE_11826chr10:126382208-126388040CD3
SE_14406chr10:126380885-126399243CD4_Memory_Primary_7pool
SE_15467chr10:126382226-126387936CD4_Memory_Primary_8pool
SE_16286chr10:126382026-126386368CD4_Naive_Primary_8pool
SE_16956chr10:126382595-126388103CD4p_CD225int_CD127p_Tmem
SE_17772chr10:126381322-126400326CD4p_CD25-_CD45ROp_Memory
SE_18306chr10:126381215-126398866CD4p_CD25-_Il17-_PMAstim_Th
SE_19113chr10:126382326-126383531CD4p_CD25-_Il17p_PMAstim_Th17
SE_19980chr10:126381909-126398610CD56
SE_20757chr10:126381300-126387847CD8_Memory_7pool
SE_22300chr10:126379671-126399931CD8_primiary
SE_25345chr10:126383270-126384260DND41
SE_26558chr10:126381993-126383146Esophagus
SE_27648chr10:126382212-126383978Fetal_Intestine
SE_28609chr10:126381970-126384134Fetal_Intestine_Large
SE_29582chr10:126381904-126383328Fetal_Muscle
SE_30910chr10:126381933-126384317Fetal_Thymus
SE_31435chr10:126381892-126383753Gastric
SE_40602chr10:126381203-126384381Left_Ventricle
SE_42109chr10:126381867-126383965Lung
SE_48059chr10:126380077-126384160Psoas_Muscle
SE_48558chr10:126381927-126383988Right_Atrium
SE_50103chr10:126381991-126384073Sigmoid_Colon
SE_51170chr10:126380959-126384345Skeletal_Muscle
SE_52350chr10:126381896-126384334Small_Intestine
SE_53300chr10:126382058-126384299Spleen
SE_55093chr10:126382110-126382658Thymus
SE_55093chr10:126382723-126383425Thymus
SE_58522chr10:126367014-126434794Ly1
SE_62212chr10:126285528-126438541Tonsil
SE_65502chr10:126381338-126383699Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10126382372126382711
chr10126383553126383804
Number: 1             
IDChromosomeStartEnd
GH10I124691chr10126380158126399793
Enhancer Sequence
CCTGGGAGGC GGACGTTGCC GTGGGCCAAG ATCACACCAC TGCCCTCCAG CCTGGCGACA 60
GTGAGACTCT GTCTCAAAAA AAAAAAAAAA AGAAAAGCAG GCACACCTCA GATGAAATCT 120
CGCTGCCTGG GTGGAGTGCA CTCCCAGTTC ATGGAGCACA CGGAGGACTG GAGAGGTAAC 180
CTGAGCTTCC ACTAGACAGA GTGCACGGGG TAAGGCTCCT GACTGCTGAC ACCCGCTCCG 240
CTCCAGCAAG CGCAGGAAAG GGATAGAGGT GGGAGGGAGG ATGTGTGCTA GTGTGTGGCC 300
GTCTCCTTAA ATCCTCACAA CTTGCAAACT GAGGAAACCT AGCCGGGAAG ATGGGGTGGT 360
ATCCCCATAG CTCAAGGGCC TCCACATCTC ACGGGAGTTG GCCTAAGCAG TGCAGAATTC 420
ACTGTTCGTT GATCTTTCTC CTCCACCAGA CAGAAAGCTC CCTGAGAGAA GGGGCAGGGT 480
CTGATTCACT CTATCCCTCA CCAGGTGCCT GACACACAGC AGGTGCTCAA GTCATATCTA 540
TGACAGCAAG CCACTGAAAA TGAAAACAAA CTGCAGTCAG TGAAACACGT CAGTGATGCA 600
CAGCCATGCA GGTCAGGGTT TTCCTGAATT AGGGAGGGGC CGACCAACAG AAAGATGAGA 660
CCCATGGAGA GAGAGCAGCA GAGGAGAACA AGGGGACTCC ACAGACCTCC CACCAGTACA 720
ACGGCTCCCC GCTTCTCCCT CTGCTGCCTG GCAGTGCCCT GGCACTGTCC CACAGAGCAG 780
AAGGAAGACA GGACCCTGCT GAAGAGGAGA AGAGCCTGGG ACGGAGGCAT TGGGACCCAG 840
CCAGCACTTC CTAAAGAGCC ACTCTGTAAA CAGGAGTCTG CAGACACAGC GTAGTCCCTC 900
CTGGAAACCA TGGCCTCCCC GGTAGAAAGC AGGTTGCTGG GCTCTGCAGC CTCCGATAGA 960
CTCTCCTGGG CCATCTGGAC TTTTTCCCAC ACACCTCCCT TCTCCGGGGC CTCTGCCTTG 1020
GTCTCTGGGC CTCAAGACCT GGCCCTACAA GGGCGACTCT CTCTGTCATC ACAAACCCAC 1080
CAGACTTCCA CCTTATTATA ACTTACACAG TGCAAAGACT AGAAATCCTT GAAATAAAGA 1140
CCAACATCTC CACAACCCAG TTTACTGGTC TGGCCCGGTT GACAGCTAAA GCCTAGGCAG 1200
GGTTGAGGGG CTGGGCATGC CGGGGCCTCT CTCTTTCCCA GCATGACGCA GGAAGGAAGC 1260
GCAAAGGTGA GGTTGTCCCA GGAAGCAGGC GAGGAGGCAG GCTTCTGAGC TATGTGTCTG 1320
GGGCCCTGAG GGTTTGCTGA AAGCTGTAAA CCACCGGGGA GGTATTCAAT CCTGTGGGGA 1380
CGGGCCTCCC AAGTATGTCA CATGGAAAAC CAGGGCCAGC TGATCTCCCT GTCTCCATCT 1440
TCTTCAGTGG CAGCATCAAG AGCACCGCCA GGTGTCCCAG AGCCATGGCA GGTGGTTGAG 1500
AAGAAAACAG TCTCCCTTCG TCACCCACCT GAGTCCAACT CCGCTTACTG AGGGACCTTG 1560
CAGAGGGCCA CCTCACTAGA CCTCAGTTCT CCCGTATGTG AATGATGCCA CTGGCAGAGC 1620
CAGCGGGGCC CAGCATGTAA GGAGCCTGGC ACAGTGCTCA ATCTGACACA TCACCTCATC 1680
TATGGCAACT GTATCTGAAG AAGAAAAACA AAACACCGCA CATGGAGGGA GGACCGAGAA 1740
GGAAAGGCAA GGGAGACTCT GAGGTCTGAC CAAAGTAACC TTTGAATCTG AAAGCCCACA 1800
GTCATCATCA TCTATCATCT GAGAGTGGTT TCTGAGTCCA CGCAGACGTT ACAGAAACTC 1860
ATCCGGCAAG ACGTCCCCAA AGGTGGGCAA GGAGAGCCAC AGAGAGACAC TGAGAGGTCA 1920
AACAATGCCC AATCATCTGA AGCATCAAGT AATCAATGGT CATCTTTTTT ACCGCCTATA 1980
AAAAACAGTA ATTCACACTT GCACAGAAAC AGAAGATCAA GGCAATCTTC TCTGGAAGGC 2040
ATGTCAGCAA AATGAATCAA GAGCCTTAAA AATGTCCCTG CCCTCCAGCC TGTCTATTCC 2100
ACTCCTGGAA ACTATCCTAG CAAATCATCA CAAAGGCAGA CAAAGAATTA GGCACTTACC 2160
TAGCCACTGT TCATCACAAC AGCAAATAAA ACAGCCTCTT GACCCAACAG CCTAGATGTA 2220
GTTACATCAC TAAAGACATT CTGATACATT TACCACCCAA TGCGGTACTG TAGACCATTA 2280