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

TagContent
EnhancerAtlas ID
HS044-07348 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr2:112251000-112252460 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nfe2l2MA0150.2chr2:112251535-112251550TGCTGACTCATTATT-6.19
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00172chr2:112245156-112256428Adipose_Nuclei
SE_01307chr2:112249522-112251663Adrenal_Gland
SE_01980chr2:112249536-112253191Aorta
SE_02250chr2:112246503-112256255Astrocytes
SE_09255chr2:112242322-112254579CD14
SE_11821chr2:112245569-112253926CD3
SE_13188chr2:112250048-112253658CD34_Primary_RO01480
SE_13332chr2:112246928-112254907CD34_Primary_RO01536
SE_14312chr2:112249042-112254777CD34_Primary_RO01549
SE_14375chr2:112242883-112255469CD4_Memory_Primary_7pool
SE_15396chr2:112247191-112253574CD4_Memory_Primary_8pool
SE_16282chr2:112246460-112254339CD4_Naive_Primary_8pool
SE_16917chr2:112248128-112253231CD4p_CD225int_CD127p_Tmem
SE_17781chr2:112242510-112254358CD4p_CD25-_CD45ROp_Memory
SE_18238chr2:112242335-112255432CD4p_CD25-_Il17-_PMAstim_Th
SE_19110chr2:112243711-112254403CD4p_CD25-_Il17p_PMAstim_Th17
SE_19985chr2:112242474-112254362CD56
SE_20734chr2:112242380-112254532CD8_Memory_7pool
SE_22092chr2:112247584-112253444CD8_Naive_8pool
SE_22299chr2:112242383-112254936CD8_primiary
SE_25382chr2:112236252-112254103DND41
SE_25821chr2:112246354-112256327Duodenum_Smooth_Muscle
SE_27273chr2:112248093-112254583Esophagus
SE_30074chr2:112249847-112256216Fetal_Muscle
SE_31329chr2:112250186-112253680Fetal_Thymus
SE_34722chr2:112246590-112256403HeLa
SE_36533chr2:112249648-112256176HMEC
SE_36949chr2:112245538-112256379HSMMtube
SE_38019chr2:112245049-112255663HUVEC
SE_38854chr2:112242450-112258192IMR90
SE_39850chr2:112248124-112254377K562
SE_42753chr2:112248050-112254756Lung
SE_43608chr2:112249704-112253980MM1S
SE_44324chr2:112243463-112259036NHDF-Ad
SE_44769chr2:112246473-112256276NHLF
SE_45566chr2:112242529-112259116Osteoblasts
SE_47156chr2:112242747-112256913Panc1
SE_50094chr2:112242440-112254761Sigmoid_Colon
SE_51387chr2:112247019-112256063Skeletal_Muscle
SE_51721chr2:112248295-112256070Skeletal_Muscle_Myoblast
SE_52359chr2:112245404-112254714Small_Intestine
SE_53336chr2:112246383-112254729Spleen
SE_55797chr2:112245331-112263554u87
SE_58089chr2:112250532-112253746VACO_9m
SE_63507chr2:112248229-112256219HSMM
SE_65208chr2:112250723-112255150NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2112251481112251757
Enhancer Sequence
TCTGGGGAGG TTTTCTTCCT TGGAATCTTG TTCTCTCATT TTAAGCTGAC TTAATCTTCC 60
CACGCTACAC GTCACATGCA GAGCGCCAAC TTTGAAGTTC ACTCGGTGAC CGACTCTCCC 120
GCCCAATCCC TCGGCGAGGG TGACGTGCAA GCGGAACATC TCAAGGCTCC AGATGCAGGC 180
TCAGCCCTCA GCTGCCCTGG CCTTAATAAA CACTAGATTT TTCATTTCAG AAACTATGTT 240
CAACCTGTTG CCTCAAGACA ACCTAAAAAT CGTCAACATT AGCCAAAGGT TGGAAGCCAA 300
ATGTGTTAGC TCCTGCCTCA GAGACAGATC CCTTAGCAGA GGGGGTCTCT CAGCAGAAGC 360
CCAGAGGAGC TGGGACCCAA GCTGGGAGCT GGTCACTTAC ATAAGGGGGG CATCCTAAGT 420
CGATTTTAAC CCGAGATCCA CCAGCCAAGC CTTCCTACGG GGGGCCGGCC AGCCACCGTG 480
CTGTGCTGAG GAGCAGATTG AACATTCTCT TAGCTGCTCC AATTTTAGAA TTGGGTGCTG 540
ACTCATTATT AACTCAGGAA GCCCACACAC TCAAATGACT GTACTGAAAA AGCTCCCTGT 600
CATACCCTGC CTACTGATGT GTTGCTTTTT AAGCAAATTT GAAAAATGTT TATCATAAGG 660
TATTTATGAC ATTTTAACCG TTTCATTTAC AGTAACTAGA ACAACATTAA AAAAAAAATG 720
TTTCCTGTAT TTTACTTGAC AGTAAAGCTA AGCTTCATCG GAATACTAAC AGCCTGAGAA 780
ATACCTATCA AGATCAAGTC AGGCCTCAAA GACTGAGTGG CCCCCTCCTC AGTCCTCCCC 840
AGTCCCCCAC CCCCAGCGCT GGCCCCCAGC ATTTTTACGT TCTTCCTGAT TTTACTACAG 900
TTTGTGACTT TCAACGTTAA GGAAAAGGAA AGGACGTAAA ATACGCTCCT GCAATCATTC 960
ATATGCTTTT AGAGAAGGCA GCCAAAGTTC TGCCTCTCTG GTATTTCTCA CACTGAAATT 1020
GGGCAGCTCT GACCACGAGG CCAGAAATGG CTCAGGAGCT GCCTCTCCTC CACCTCTGAG 1080
AAGCGGAAGC TCACCCAACC TCAGCAACCC TGGGTTAGCA CAAGTATACC CACTTCCATC 1140
TCTGAGCTTC ACTTTGGCTT CTCAGAGGAG TCCCGAGCAG CTTATTTTCC AGCCAAGCAC 1200
TGCAGTCTCT TCCAAGACAA CAGAAGGTGC AACCGGCATC TACATTCTTA CAACGAAGGA 1260
CTGAGAAACA CCTCCTGACA GTCACACTAC AGGACAGTAA CCATGGGGCT GGTGACAGAG 1320
GCAGCCACTT TTCTAAAACG ACAGATCTTC AAAGTCTGAA AGAAACGCAG TGTCCTCACC 1380
AGGACGCAGC AGCCTTTCCC ACAGCCCAGA CTCCAAGGCA AACTGCAGAA GCAACCCTAA 1440
AAATGACAGA AACATACTCA 1460