EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-24644 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr5:131794400-131795880 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr5:131795063-131795074TGGGTGTGGCC-6.62
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00037chr5:131790656-131796338Adipose_Nuclei
SE_01257chr5:131794641-131795249Adrenal_Gland
SE_09163chr5:131788117-131797621CD14
SE_10340chr5:131790824-131795464CD19_Primary
SE_10915chr5:131787711-131797453CD20
SE_11856chr5:131788689-131797117CD3
SE_13479chr5:131790641-131796411CD34_Primary_RO01536
SE_14495chr5:131789106-131797177CD4_Memory_Primary_7pool
SE_16304chr5:131790613-131795606CD4_Naive_Primary_8pool
SE_16894chr5:131794286-131795229CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131789423-131795425CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131787920-131797394CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131787905-131797327CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131790791-131797009CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131788439-131797324CD56
SE_20775chr5:131790546-131796689CD8_Memory_7pool
SE_21960chr5:131790607-131795345CD8_Naive_8pool
SE_22284chr5:131788012-131797561CD8_primiary
SE_23079chr5:131794575-131796517Colon_Crypt_1
SE_23750chr5:131794696-131796088Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131790957-131797727Duodenum_Smooth_Muscle
SE_26597chr5:131794257-131796075Esophagus
SE_27629chr5:131790763-131801421Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131790670-131796844Fetal_Thymus
SE_31393chr5:131794548-131796995Gastric
SE_37771chr5:131791257-131796632HSMMtube
SE_39368chr5:131791092-131797698Jurkat
SE_40726chr5:131794433-131796690Left_Ventricle
SE_42103chr5:131794463-131796999Lung
SE_43869chr5:131790540-131795910MM1S
SE_50023chr5:131791250-131797789RPMI-8402
SE_50051chr5:131790768-131797132Sigmoid_Colon
SE_52336chr5:131790812-131797015Small_Intestine
SE_53285chr5:131790524-131796944Spleen
SE_55171chr5:131794927-131796428Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131794596-131795860Pancreatic_islets
SE_66244chr5:131791092-131797698Jurkat
SE_67186chr5:131790540-131795910MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5131795209131795478
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
ACATTTTTGC CAACCATAGA TATTTTCTAT CTTTTTCATG TTAGCCATTC TGGCAGGTAT 60
GTAGTGGTAT CACAGTGTGG TTTGAATTTG CATTTCCCTG ATGACTAATA CAGCTGAGCA 120
ACCTTTCATA TGTTTGTTAG CCATTTAGAT CTTCTCTTTG CAAAGTGCCT GTTGGAATAT 180
TTGGACATGA GTATTTTTAA AAAGCTCCTT AGGTAACTCT ACTGTGTAGC CAAGGTGGAA 240
AACCACTGAA CTAAAACCAC AAATTAGTAT CTGCGTCTCC CTTTCTTCAT GATTTGCCTT 300
TGAACTTAGA GCATTTTGGA TCTGAGAGGA CCTCGTGGAA CTGGGAAAAG ATTATATTCA 360
CTCCCTACTA AGATGAGCCT GTCAGGAAGA AGCAATTGGA GCTGGCAGTT AAGAATCTTT 420
AGGAATGTGA CCTCTACTTC AGAAGGGTCC AGGGAGGGCC TGTGGTGTCC ACAGCTGCCA 480
CAGACATTTC CTAACCACAA AAATGGCCCC TTGGTGGTCT CCCCAGAGCT CCAGGCAGTC 540
ATGGGGAGGA AGCGGAGGGC CCCATGCCAG GTACTTCCCA GTTTCTAGGC CAACATGAAT 600
GGGACACAGC TCATATGGGG TTGTGGTTAG ACTGGGGACA GTGGAGCATA TGTTCTGGGG 660
ACCTGGGTGT GGCCAAGGGA GGCCTCCTGT CTGTGGCCTT TGTCCCAGAT TGGAAATCAG 720
CCAGTGGGGC TCTCCTACAT GGGTCCAGGC CTGGCTAGCT CTTGAATTCT GTGCGTTTGC 780
ATGTGGGTCC TTATGCATGC GTCCTAGAGC AGGGTCCCAG GGGGCCACTC CCCCCCCCGA 840
CCCCTTACTC CTCTAAGCTG GGAAACACGT GGCATGAGAG AACACACTGT GGCTTCTAAT 900
GACATCGTGT CTTGATTGCA TCCCCATTGC ATCATCTGGG CTCATCTCAT CCCCACCTCT 960
GGACTGTAAC ATCATCCCAG GGACTGCCGG ACACTCATCT GTGCTCCCCC ACAGAGAGTA 1020
TAATGCCATT TGGTAATTCA GTACAGCCTC TTCCAACTTG AGAAAGAAGA TGCATTTCCT 1080
TCCCTCAGTC TTGAGCTGTG CAGGTGTCAC GCTGAGCTGC CCTGTGTGGG CTCCATGTTG 1140
GCACACATCG GTTGCAAGGG GCTCTGTGTA GTGAGTCTGG AGTTGGACCA CTGGCCAGGC 1200
GCTGGGATGC TAGTGCCTGG ACTGAGTGTG CACAGAGGCC CCTCAGGCAG AGCCACAGTG 1260
GGCGCTGAAC CTCCTGGTGA AGTTCACCGC AGTAACTAGA GCTCAGTGGG AGGGGCTGGC 1320
CTATCAGCAC CTGTCCTGTG TGCTTTTTGA AAAGAGCAGG GTCTACCTTC TGTCAACTGA 1380
AGTCCTGCCA GCTGCATGGC ATGAGATGAG GGACAAAGTG GCACGTGAAC AAAGTTGACA 1440
TTTTGGAGGC TGTTAGGCTC AGAGCCAACC CTGGGCTCCA 1480