EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS018-02379 
Organism
Homo sapiens 
Tissue/cell
CD19+ 
Coordinate
chr10:3852770-3854590 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Arid3bMA0601.1chr10:3853126-3853137CTAATTAATAT-6.02
Foxa2MA0047.2chr10:3853372-3853384CCTGTGTAAACA-6.14
IRF8MA0652.1chr10:3853764-3853778CAGAAACCGAAACT+6.64
IRF9MA0653.1chr10:3853763-3853778ACAGAAACCGAAACT+6.94
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00402chr10:3845037-3857309Adipose_Nuclei
SE_11882chr10:3844923-3855094CD3
SE_13060chr10:3852925-3853909CD34_Primary_RO01480
SE_13486chr10:3850098-3854219CD34_Primary_RO01536
SE_14165chr10:3851846-3854211CD34_Primary_RO01549
SE_14454chr10:3844440-3855702CD4_Memory_Primary_7pool
SE_15590chr10:3851015-3854890CD4_Memory_Primary_8pool
SE_16065chr10:3851752-3853079CD4_Naive_Primary_7pool
SE_16325chr10:3844818-3854942CD4_Naive_Primary_8pool
SE_16945chr10:3845071-3854779CD4p_CD225int_CD127p_Tmem
SE_17898chr10:3842562-3855349CD4p_CD25-_CD45ROp_Memory
SE_18262chr10:3843866-3855308CD4p_CD25-_Il17-_PMAstim_Th
SE_19252chr10:3844144-3855295CD4p_CD25-_Il17p_PMAstim_Th17
SE_20116chr10:3844478-3854992CD56
SE_20771chr10:3844502-3855029CD8_Memory_7pool
SE_21756chr10:3850720-3854675CD8_Naive_7pool
SE_22443chr10:3844580-3856035CD8_primiary
SE_25500chr10:3843057-3856858DND41
SE_26256chr10:3844553-3854705Duodenum_Smooth_Muscle
SE_35818chr10:3845057-3856086HMEC
SE_37615chr10:3851700-3854642HSMMtube
SE_38247chr10:3845355-3854596HUVEC
SE_40296chr10:3850766-3854220K562
SE_41340chr10:3847447-3854927Left_Ventricle
SE_42946chr10:3847414-3854892Lung
SE_44151chr10:3852091-3854825NHDF-Ad
SE_44780chr10:3850822-3854622NHLF
SE_45602chr10:3850824-3857124Osteoblasts
SE_47115chr10:3844078-3857005Panc1
SE_50955chr10:3853236-3854755Sigmoid_Colon
SE_51836chr10:3851874-3854622Skeletal_Muscle_Myoblast
SE_52694chr10:3847404-3854725Small_Intestine
SE_55908chr10:3852080-3854527u87
SE_57501chr10:3853185-3854669VACO_503
SE_58236chr10:3853408-3854001VACO_9m
SE_63160chr10:3844860-3855094Tonsil
SE_63583chr10:3846087-3854622HSMM
SE_64398chr10:3845568-3854714NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1038533933854169
Number: 1             
IDChromosomeStartEnd
GH10I003802chr1038445943855677
Enhancer Sequence
CATTTTGACC CTAATTTCAC TTACAACTTT CTCATAAGAT ACTGTTAGGA GTGAAAAGCC 60
ACAATTAGCT CTAGGCCAAG AGTGAATAAT TTCAACAGCC TCTCTAAGAT GGTTTATATT 120
TTTGGAGCCA TATATGGGTG AAAGTAACGA TTTCCACAGG AGGACAAACA AAAGGAGATT 180
TTTGCACACA ACAGGGAAAA GAAAAAGGTT TAAACTTTCA CATGTGAAAA AGTTCAAATT 240
CCCAAGCCTT GCTGAACACA ACCCCAGGTA GTTTTAAAAT TTGCTTTCAA TAAAAATTTA 300
TTTGAAATGA AATGCTTTAC TAACTTTCAT GGCTAAATCA GGAAACACCG TTTTCACTAA 360
TTAATATTAA ACAGTTGGCG AGCACAGCAC TTCTGGATGT GTTCCTTCTT CATAACTAAA 420
AATGAGTGAA ATTGTAATTG AATTCTGATG ATAATCTTAA TAGCATCATT CTCTACGTTG 480
ACTCCTTAAA GCAATTTTAT ATTTGCAAAT TGTCTTTGCC TTCCTTTTAG CTTAGTTATA 540
TAGCTTGCTT TGCTCAAAGA GTAAAATTAA AGTCTTAACT AATGTCAAAT GGTTTTGCTT 600
TTCCTGTGTA AACATAAATA TGTTAAGAAA TGTATAGTAA GTTATCTTAT TTTAATAGAG 660
ACTCATCAGT GCTAGTTATT TAGTGCCTCT CAATAGTATT TCTGGCAAAC TGCACATGGC 720
CTTCCTCATA GAATGAGGAG TGGGCATTGA CATGAATTTC TAAATTGTGG CATTTCCTGG 780
CATGATGTCA GTTGGCTTAA TCATCTCAAC TGTCAGCTCA CACCCTTGAC AGCCAGCTCG 840
GGAGCTGGGG AGAGTCCAAA TTTGGTGTTC TGAAGGAGCT CACAGGGGTC TCTGGCACGT 900
AATGATCACC TTGAAAGTCA TCGATTTCAA AAAGAACATT CCACTGTGGA AGAGCAGCCA 960
AGAGAAGCAA ACCTCAGGCA CACACAGTCT GTAACAGAAA CCGAAACTCC TAGCAGGAAA 1020
ATACCATGAC CTGCAGTGAC AGGGCCAGAC CATTTCAGTG AACTCAGCAT GCAGAACTGT 1080
GTGGGGAAGG GCCCCATGAG AGAGTTACTA TGATTATTAT TAAGAGGTGA AAAACATTCT 1140
CTAAAATGGT GCGGTGTCAG AGTTAGTTTC CAGAAGGCTT GCTAACCTGC AGGGGCTGGG 1200
GTAGAAAGTC ATTCTATAAA AGGCATAGGT GCAGCTGTGA CTTCGAACGT TTCCCTGTGG 1260
ATGAGATGCC CACACATTTC AGGACACATG TACTATGACG TTTTGGGTGC AGAGAAACGC 1320
TGCACCAATC ACTCAGCTCC TGTCTCTCTG CCATCAATTT TGTCAAATGT CAAAAATCAT 1380
CTATTCAGAG ATGCCTATGT AGAACAGAGG AGGGGACTCT GAGTATTTAG GAATCAGTTT 1440
CCTAACTCAG CTCATCACCC TCTCACTCAG GACAACTTCC GCTTGCCTAG TGGGGAGAAG 1500
CTTCCAAGTG CAGTGTGGGC ACTGGAGGGA ATGCCTCGGC CACAGTTCCC GTGGAAATCT 1560
CGGGGATTTA AGTCTTTAAC CAGCCCCCCA AAGACCACAA CCCTCCCTCC ACCATCCACT 1620
GACAGCTTTC TTGGCTCCCT AAGCTGTTCT GCACTGAGTC CTCAACTTAT CTTCTCTGCT 1680
GACATTTCCC CTAGTTGTGG TGGTCATGCC CGCCAGGGAG CTGCTCCCTC TGAAGGTGAT 1740
CCTGCCCCAT CTCCGGGCCT CACGGGCATG GCTGCTCCAA AGACCGCGAC CAATTTCCTC 1800
CTCTAAATCA CGTGGGATGC 1820