EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS054-00048 
Organism
Homo sapiens 
Tissue/cell
FT246 
Coordinate
chr1:12212940-12214360 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr1:12213290-12213301TGTGACTCATC+6.14
JUNDMA0491.1chr1:12213290-12213301TGTGACTCATC+6.14
Nr2f6(var.2)MA0728.1chr1:12214116-12214131AAGGTCAGGAGTTCA+6.04
SPICMA0687.1chr1:12213408-12213422TTCTTCCTCTTTTG-6.62
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00369chr1:12212169-12214461Adipose_Nuclei
SE_01471chr1:12212830-12213765Adrenal_Gland
SE_09154chr1:12199965-12214486CD14
SE_10696chr1:12207898-12214373CD19_Primary
SE_11902chr1:12208865-12214231CD3
SE_14553chr1:12208809-12214332CD4_Memory_Primary_7pool
SE_15480chr1:12208768-12214030CD4_Memory_Primary_8pool
SE_16369chr1:12212506-12213878CD4_Naive_Primary_8pool
SE_16946chr1:12210087-12214122CD4p_CD225int_CD127p_Tmem
SE_17650chr1:12208923-12214185CD4p_CD25-_CD45RAp_Naive
SE_17827chr1:12206501-12214454CD4p_CD25-_CD45ROp_Memory
SE_18389chr1:12206868-12214379CD4p_CD25-_Il17-_PMAstim_Th
SE_19117chr1:12208827-12214340CD4p_CD25-_Il17p_PMAstim_Th17
SE_20048chr1:12207907-12214477CD56
SE_20873chr1:12208284-12214108CD8_Memory_7pool
SE_22347chr1:12207903-12214404CD8_primiary
SE_26251chr1:12206411-12213727Duodenum_Smooth_Muscle
SE_27503chr1:12212703-12214088Esophagus
SE_30788chr1:12212889-12214071Fetal_Muscle
SE_32030chr1:12212751-12214118Gastric
SE_38661chr1:12212782-12214329HUVEC
SE_41498chr1:12212621-12214203Left_Ventricle
SE_42336chr1:12209781-12214078Lung
SE_48967chr1:12212801-12214137Right_Atrium
SE_50250chr1:12207958-12214180Sigmoid_Colon
SE_52522chr1:12206320-12214007Small_Intestine
SE_53313chr1:12206186-12214442Spleen
SE_55394chr1:12212891-12213422Thymus
SE_59216chr1:12197780-12224862Ly3
SE_61096chr1:12184746-12245090HBL1
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11221312812213883
Number: 1             
IDChromosomeStartEnd
GH01I012140chr11220016112214656
Enhancer Sequence
AATTTACCAC TCATTCCTAG GAGCTAAAGG TTCCTGGGTT CCTCCTTGGG GCACATGTCT 60
AGGAGCAGGA TCTCGATCTG GTGGCAGAGG GGCAGCAGCT GCTCCGTCTG GCATACAGTA 120
GGTGCTCAGT AAGTCTGCGG GGCAGGCAGG ACAAGCCTGG GTTGGAAGGA GGTCCAGTTT 180
CTTGGGAGTG AGAGCCTCAA GACCAACTTC ACCTGAAGGA CAAATGAGAG GTGGCCGAAT 240
CACTGCCAGC TACTTCAAGA AGCCCCTAGG ACACTCCAGC CAAGGTGCCT TGGTCCCTTT 300
TCTAAGTCGC CTGCCCACCC TGCCCAAGCT CCTGCGGGGA GTGTGCCCAC TGTGACTCAT 360
CCACGCCCAG CCCTGCCCAG CTCTCACTGG GGCAGCAGTA GGCACACATA CTCGTAAAAG 420
TCTGAATAAG TGAAGACTGG GAAATTGCAC CAGGGAAAAA CTACTTATTT CTTCCTCTTT 480
TGAATTGGGG AGGGGAAATG TTGCGGGGGA AATGAGGTCA GTGACGTGGT GAGCATTTCA 540
TGCTCCTTAC TGATGAGCAG AGGGCCGGTA TCACGTGCTG CCTTCCTAGG GAGGGCTGGG 600
TAGTGCGTCA AGGAAATGGG CCCAGAGCTG TGTCTCGTCC AGTCTAGCAG GAAACTGCCC 660
ATCTCACTGT GTCACTCCCT TCTCTGTCCT TGCTCTAAGC CTCTACCCTG ACTGCCCTTG 720
CTCTGAGCTG AAATCTCACT AATGAGAAAA AAATGTGCTG GTTTATGCCT CTGTGGGCTG 780
GCTGGGCTGG TAGGTCCCAG GGGGCAGCAT GGCCTGGAGG AAACCGAGTG CACGGGGCAA 840
GGATGATGTG CACGAGTGGT ATGTGACTCC CAGGGCTCAC AGCCTCATGC AGCCCCTCCC 900
TCTGAGAGTA TAGATGGGGA AACTGAGGCC TGAGAAGGCG AGAGATGTGC CTGAGGTCAC 960
ACAGAGAATC CGTGGCCCTC AGCACAAGCA CCCAGTTTGC TGGTACTTTA AAGATAAAAA 1020
TAAACAAACT TTATAAATGG AAAAGATGAA TAAAAGAAGA AACGAAGTAT AAGGAATATG 1080
ATAAATATAA TAAAAATTAC ACACAATCTT GGCGAGGCAC AGTGGCTCAT GCTAGTAATC 1140
CTAACACTTT GGGAGGCCCA GATGGGCAGA TCATTTAAGG TCAGGAGTTC AAGACCAGCC 1200
TGGCCAACAT GGTGAAACCC CATCTCTACT AAAAATACAA AAATTAGTTG GGCATGGTGG 1260
TGCGCGCCTG TGGTCCCAGC TACTTGGGAG GCTGAGGCAC GAGAATCACT TGAACCCAGC 1320
AGGCGGAGTT TGCAGCAAGC TGAGATCACG CCACTGCACT CCAGCCTGGG TGATGCAGCC 1380
AGACCAAGAC CTTGTAACAA CAACAACAAA AGTAAAACAA 1420